(c) What does the bar code look like? Prevention of primary and secondary carnitine deficiency due to detoxification, Levodopa 100 mg + Carbidopa 25 mg, Levodopa 250 mg + Carbidopa 25 mg, Levodopa 50 mg + Carbidopa 12.5 mg + Entacapone 200 mg, Levodopa 100 mg + Carbidopa 25 mg + Entacapone 200 mg, Levodopa 150 mg + Carbidopa 37.5 mg + Entacapone 200 mg, Levodopa 200 mg + Carbidopa 50 mg + Entacapone 200 mg, Levonorgestrel 0.15 mg + Ethinylestradiol 0.03 mg, Lidocaine 2% + Adrenaline 1:80,000 (12.5 microgram/mL), For patients with type 2 diabetes mellitus and chronic kidney disease stages 3b, 4 or 5, Treatment of patients with culture-positive vancomycin-resistantenterococci (VRE) bloodstreaminfections, Treatment of patients with culture-positive vancomycin-resistant enterococci (VRE) bloodstream infections, Magnesium Carbonate 150 mg/5 mL + Sodium Bicarbonate 250 mg/5 mL + Aromatic Cardamom Tincture 0.15 mL/5 mL, Magnesium Chloride Hexahydrate, Potassium Chloride & Procaine Hydrochloride, Magnesium Chloride Hexahydrate 162.5 mg/mL (0.8 mmol/mL) + Potassium Chloride 59.5 mg/mL (0.8 mmol/mL) + Procaine Hydrochloride 13.64 mg/mL (0.05 mmol/mL), Magnesium Trisilicate 5% + Magnesium Carbonate 5% + Sodium Bicarbonate 5%, Attention deficit hyperactivity disorder in children and adolescents aged < 18 years old, Methylphenidate Hydrochloride (Medikinet). Treatment of hyperphosphataemia in patients with chronic kidney disease who have persistent hyperphosphataemia despite optimising treatment with calcium-based phosphate binders, or who are unable to tolerate calcium-based phosphate binders due to hypercalcaemia. (ii ) Effects of drug on the breast-fed child. Protect your familyby booking a flu vaccine as soon as possible. 15, 1980; 45 FR 72118, Oct. 31, 1980, as amended at 48 FR 37620, Aug. 19, 1983; 81 FR 60212, Aug. 31, 2016]. The headings (e.g., "Directions") are set in 8 point Helvetica Bold Italic, left justified. Caffeine acts by blocking binding of adenosine to the adenosine A 1 receptor, which enhances release of the neurotransmitter acetylcholine. Alternatively, it may be administered in a dilute solution, e.g., 5%, as a high volume enema. The article presently recognized in The National Formulary under the heading "Estradiol" and which is said to be "17-cis-beta estradiol" is the same substance formerly recognized in the United States Pharmacopeia under the designation "Alpha Estradiol." Treatment of FLT-3-mutation positive acute myeloid leukaemia (AML) in combination with standard intensive induction and consolidation chemotherapy. Animal doses or exposures must be described in terms of human dose or exposure equivalents and the basis for those calculations must be included. 16, 1979]. 2) in area and should be separated from each other by at least 0.8 cm. (12) Total surface area available to bear labeling means all surfaces of the outside container of the retail package or, if there is no such outside container, all surfaces of the immediate container or container wrapper except for the flanges at the tops and bottoms of cans and the shoulders and necks of bottles and jars. Avoid getting into the eyes or on mucous membranes." The Food and Drug Administration will identify these situations in direct correspondence with the drug promoters, after which the failure to make the disclosure will be regarded as misleading and appropriate action will be taken. (2 ) Risk statement based on animal data. Sec. If the drug is expected to affect labor or delivery, the labeling must provide information about the effect of the drug on the pregnant woman and the fetus or neonate; the effect of the drug on the duration of labor and delivery; any increased risk of adverse reactions, including their potential severity and reversibility; and must provide information about available intervention(s) that can mitigate these effects and/or adverse reactions. If more than one active ingredient has the same purpose, the purpose need not be repeated for each active ingredient, provided the information is presented in a manner that readily associates each active ingredient with its purpose (i.e., through the use of brackets, dot leaders, or other graphical features). Re-induction with ipilimumab is not allowed. In addition, the warning statement shall appear on any labeling that contains warnings and, in such cases, the warning statement shall be the first warning statement under the heading "Warnings.". This subsection of the labeling shall be based primarily on human data and human experience, but pertinent animal data may also be used. 2013 Jan;45(1):2-13. doi: 10.1016/j.jpainsymman.2012.02.008. If the Commissioner finds that there is evidence of significant incidence of fatalities or serious injury associated with the use of a particular prescription drug, he may withdraw this exemption by so notifying the manufacturer, packer, or distributor of the drug by letter. The information under these headings may appear highlighted. 7. 201.19 Drugs; use of term "infant". (e) A person performs an operation listed in paragraph (b) of this section only if the operation is performed, including the performance of the appropriate in-process quality control operations, except laboratory testing of samples taken during processing, as follows: (1) By individuals, a majority of whom are employees of the person and, throughout the performance of the operation, are subject to the person's direction and control; (2) On premises that are continuously owned or leased by the person and subject to the person's direction and control; and. (6) The letter height or type size for all labeling information, headings, and subheadings set forth in paragraphs (a), (b), and (c) of this section must be a minimum of 8 points, except for labeling information that is on or within the package from which the drug is to be dispensed, which must be a minimum of 6 points. (3) If the labeling contains any representation in a foreign language, all words, statements, and other information required by or under authority of the act to appear on the label or labeling shall appear on the labeling in the foreign language. Because it has antimicrobial and antiviral properties, it is widely used in FDA approved wound and burn treatments. The warning is not required to be included on each blister unit. Oral formulations of bisacodyl are only 16% bioavailable. and who are given concomitant standard medical management including the maximum tolerated dose of beta-blocker therapy, angiotensin converting enzyme inhibitors and aldosterone antagonists, unless contraindicated or not tolerated. Composition of the Padimate O/oxybenzone SPF Standard. Some question has arisen whether, for the purposes of drug labeling, an infant means a child up to 1 year of age or a child up to 2 years of age. Reject test data for a test subject if erythema is not present on either the unprotected or protected test sites; or erythema is present at all subsites; or the responses are inconsistent with the series of UV doses administered; or the subject was noncompliant (e.g., the subject withdraws from the test due to illness or work conflicts or does not shield the exposed testing sites from further UV radiation until the MED is determined). The Food and Drug Administration is limiting the amount of sodium phosphates oral solution to not more than 90 mL (3 ounces (oz)) per OTC container because of the serious health risks associated with the ingestion of larger than intended doses of this product. If, however, the drug is converted, compounded, or manufactured into a dosage form limited to prescription dispensing, no exemption shall thereafter apply to the article unless the dosage form is labeled as required by section 503(b) and 201.100 or 201.105. 2 10 60800 608000. Adverse reactions important for other reasons (e.g., because they are serious or frequently lead to discontinuation or dosage adjustment) must not be repeated under this heading in Highlights if they are included elsewhere in Highlights (e.g., Warnings and Precautions, Contraindications). 1 A drug subject to 201.100 or 201.105, shall be exempt from section 502(f)(1) of the act if shipped or sold to, or in the possession of, persons regularly and lawfully engaged in instruction in pharmacy, chemistry, or medicine not involving clinical use, or engaged in law enforcement, or in research not involving clinical use, or in chemical analysis, or physical testing, and is to be used only for such instruction, law enforcement, research, analysis, or testing. (20 deg.C.). (i) Overdosage. (7) 6 Adverse reactions. (5) Any risk information that is required under 201.57(c)(9)(iv) is considered "appropriate pediatric contraindications, warnings, or precautions" within the meaning of section 505A(l)(2) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. (2) If appropriate, other important chemical or physical information, such as physical constants, or pH, shall be stated. (i) This section must include the following information when the conditions listed are applicable: (A) If the drug is used for an indication only in conjunction with a primary mode of therapy (e.g., diet, surgery, behavior changes, or some other drug), a statement that the drug is indicated as an adjunct to that mode of therapy. Sec. A graphic appears at the bottom of the first panel leading the reader to the next panel. Cardiac arrest was noted in several instances. This warning statement shall appear in the "Precautions" section of the labeling. Conclusions based on animal data but necessary for safe and effective use of the drug in humans must be identified as such and included with human data in the appropriate section of the labeling. "Drug Facts" is set in 14 point Helvetica Bold Italic, left justified. Recent studies have demonstrated that sulfites may cause allergic-type reactions in certain susceptible persons, especially asthmatics. (3) Laboratory tests. The letter height or type size for the headings in paragraphs (c)(2) through (c)(9) of this section shall be the larger of either 8-point or greater type, or 2-point sizes greater than the point size of the text. For animal data, the labeling must describe the following: Types of studies, animal species, dose, duration and timing of exposure, study findings, presence or absence of maternal toxicity, and limitations of the data. (a) The label of any oral drug preparation intended for sale without prescription and which contains any salicylate ingredient (including aspirin, salicylamide, other salicylates, and combinations) must conspicuously bear, on a clearly contrasting background, the warning statement: "Keep out of reach of children [highlighted in bold type]. 552(a) and 1 CFR part 51. 17, 1999; 65 FR 8, Jan. 3, 2000; 68 FR 18869, Apr. (a) The appropriate FDA Center Director may grant an exception or alternative to any provision listed in paragraph (f) of this section and not explicitly required by statute, for specified lots, batches, or other units of a human drug product, if the Center Director determines that compliance with such labeling requirement could adversely affect the safety, effectiveness, or availability of such product that is or will be included in the Strategic National Stockpile. In the emergency treatment of these poisonings, ipecac syrup is considered the emetic of choice. If it is intended for administration by parenteral injection, the quantity or proportion of all inactive ingredients, except that ingredients added to adjust the pH or to make the drug isotonic may be declared by name and a statement of their effect; and if the vehicle is water for injection, it need not be named. Rinse with water to remove.". The labeling of all systemic drug products intended for human use indicated to treat a bacterial infection, except a mycobacterial infection, must bear the following statements: (a) At the beginning of the label, under the product name, the labeling must state: To reduce the development of drug-resistant bacteria and maintain the effectiveness of (insert name of antibacterial drug product ) and other antibacterial drugs, (insert name of antibacterial drug product ) should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. This subsection must be based primarily on human data and human experience, but pertinent animal data may also be used. The Broad Spectrum SPF statement shall appear as continuous text with no intervening text or graphic. If you do not know if you or your sex partner is infected, choose another form of birth control". The information must include, as appropriate: (i) The strength or potency of the dosage form in metric system (e.g., 10 milligram tablets) and, if the apothecary system is used, a statement of the strength in parentheses after the metric designation; (ii) The units in which the dosage form is ordinarily available for prescribing by practitioners (e.g., bottles of 100); (iii) Appropriate information to facilitate identification of the dosage forms, such as shape, color, coating, scoring, imprinting, and National Drug Code number; and. For Infusion, Azithromycin Film-Coated Tablets 500mg Lesvi Lab, Baloxavir Marboxil 40 mg Film Coated Tablet, Beclometasone Dipropionate 100 mcg & Formoterol Fumarate Dihydrate 6 mcg/Dose Inhalation, Foster 100/6 mcg/Dose Pressurised Inhalation Solution, Foster Nexthaler 100 Micrograms/6 Micrograms Per Dose Inhalation Powder, Benzalkonium Chloride 0.02%, Cetrimide 0.2% & Zinc Oxide 10% Cream, Benzalkonium Chloride 0.02%, Cetrimide 0.2% & Zinc Oxide 10% Cream 100gm, Benzalkonium Chloride 0.02%, Cetrimide 0.2% & Zinc Oxide 10% Cream 50gm, Benzydamine Hydrochloride 0.15 %W/V Gargle, Benzydamine Hydrochloride 3 mg & Cetylpyridinium Chloride 1.33 mg Lozenges, Benzydamine Hydrochloride 3mg & Cetylpyridinium Chloride 1.33mg Lozenges, Benzyl Benzoate, Zinc Oxide, & Balsam Peru Ointment, Benzyl Benzoate, Zinc Oxide, & Balsam Peru Suppository, Beta Carotene 20%,Ascorbic Acid 97% DC Granules,Vitamin E 50%,selenium fumarate 0.2% Caplet, Betamethasone 0.05% & Gentamicin Sulphate 0.1% Cream, Betamethasone 17 - Valerate 0.01 - 0.05 % Cream, Betamethasone 17 - Valerate 0.1 % Ointment, Betamethasone Dipropionate 0.05% & Gentamicin Sulphate 0.1% Cream, Betamethasone Dipropionate 0.05% & Salicylic Acid 3% Ointment, Betamethasone Dipropionate 5 mg/ml & Betamethasone Disodium Phosphate 2 mg/ml Injection, Betamethasone Disodium Phosphate & Neomycin Sulphate Eye & Ear Drops, Betamethasone Sodium Phosphate 1 mg/ml & Gentamicin 3 mg/ml Eye And Ear Drops, Biotin 0.06mg,Cholecalciferol 400IU,Cupric sulphate pentahydrate 0.1mg,Cyanocobalamin 15Mcg,Folic acid 0.80Mcg,Inositol 7.5 mg,Lecithin 50mg,Magnesium sulphate 2mg,Manganese sulphate monohydrate 0.33mg,Nicotinamide 25mg,Potassium 5mg iodide,Pyridoxine 5mg,Riboflavin 5mg,Ginseng / panax ginseng 50mg,Zinc sulfate monohydrate 0.9mg,Thiamine mononitrate 12mg,Selenium 50Mcg,Coenzyme q10 (ubidecarenone) 30mg,L-lysine hydrochloride 0.3mg (Softgel Capsule), Proviton Multivits Coq10-Se Plus Softgel Capsule 30'S, Proviton Multivits Coq10-Se Plus Softgel Capsule 72'S, Proviton Multivits Coq10-Se Plus Softgel Capsule 90'S, Borax 0.3 %W/V, Hamamelis Water/Witch Hazel Water 5 %W/V & Boric Acid 1.3 %W/V Eye Drops, Caffeine 100 mg & Ergotamine Tartrate 1 mg Tablet, Cajuput Oil (Melaleuca Leucadendron) 100 ml Liniment, Calamine With 0.25 - 0.5 % Menthol Lotion, Calcium 1000mg, Magnesium 400mg, Zinc 15mg, Copper 1mg Tablet, Gnc Calcium, Magnesium, Zinc With Copper Tablet, Calcium Ascorbate 1000 mg, Hesperidin 25 mg, Bioflavonoid Complex 100 mg & Rutin 50 mg Tablet, Kordel`S C Time Acid Free C 1000mg Tablet, Calcium carbonate 300mg , magnesium chloride 177mg, Vitamin C 20mg , Vitamin E 3mg, sodium selenite 0.04mg, Lactobacillus acidophillus 25%, fiber, citric Oat Bran and whey Capsule, Calcium Carbonate, Cholecalciferol 600mg Film-coated tablet, Flavettes Cal D3 600mg Film-Coated Tablet, Calcium Chloride Dihydrate 1.98 mg/ml, Magnesium Chloride Hexahydrate 0.91 mg/ml, Sodium Chloride 4.21 mg/ml, Dextrose Anhydrous 9.01 mg/ml, Sodium Chloride 6.18 mg/ml & Sodium Bicarbonate 3.59 mg/ml Haemodialysis/Haemofiltration Solution, Hemacom Lf (Continuous Renal Replacement Therapy Solution Without Lactate), Calcium lactate pentahydrate 300mg Tablet, Royce Khaltate Calcium Lactate 300mg Tablet, Camphor 10%,Methyl salicylate 60%,Clove oil 6% (Eugenia Caryophyllus (Clove) Flower Oil), Camphor 10%w/w, Menthol 12%w/w Liquid solution, Camphor 10%w/w, Methyl Salicylate 10%w/w, Menthol 9%w/w 17.5gm, Balsem Gosok - Balsem Merah Cap Betet 17.5gm, Camphor 11 %W/W, Menthol 10 %W/W, Cajuput Oil (Melaleuca Leucadendron) 7 %W/W, Dementholised Mint Oil 6 %W/W, Clove Oil 5 %W/W & Methyl Salicylate 10 %W/W Ointmen, Camphor 4%w/w, Methyl Salicylate 10%w/w, Menthol 9%w/w, Eucalyptus Oil 10%w/w 17.5gm, Balsem Gosok - Balsem Hijau Cap Betet 17.5gm, Camphor 4%w/w,Menthol 10%w/w Ointment 20gm, Camphor 4%w/w,Menthol 10%w/w Ointment 36gm, Camphor 40 mg, Capsaicin 0.75 mg, Menthol 100 mg & Methyl Salicylate 40 mg Cream, Camphor 5%,Menthol 5%,Wintergreen Oil 60%,Mentha piperita (Peppermint Oil) 10% Liquid 12ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil 15%w/w Medicated oil 10ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil 15%w/w Medicated oil 14ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil 15%w/w Medicated oil 28ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil 15%w/w Medicated oil 3ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil 15%w/w Medicated oil 56ml, Camphor 5%w/w,Menthol 16%w/w,Methyl salicylate 15%w/w, Eucalyptus oil15%w/w Medicated oil 5ml, Camphor 5%w/w,Menthol 9%w/w,Methyl salicylate 18%w/w Ointment 20gm, Camphor 5%w/w,Menthol 9%w/w,Methyl salicylate 18%w/w Ointment 36gm, Camphor 7%w/w,Menthol 7.5%w/w,Methyl salicylate 13.5%w/w Ointment 20gm, Camphor 7%w/w,Menthol 7.5%w/w,Methyl salicylate 13.5%w/w Ointment 36gm, Carbinoxamine Maleate 4 mg & Pseudoephedrine HCL 60 mg Tablet, Carbocisteine 20 mg & Promethazine Hydrochloride 0.5 mg Syrup, Carbocysteine Lysine Salt 2.7G Powdered Sachet, Cefadroxil Monohydrate 125 mg/5 ml Suspension, Anprodroxil Granules For Oral Suspension 125mg/5ml, Cefoperazone 500 mg & Sulbactam 500 mg Injection, Supraxone 1G (Ceftriaxone Powder For Solution For Injection/Infusion), Axcel Cefuroxime-125 For Oral Suspension (125mg/5ml), Cephalexin Monohydrate 125 mg /5 ml Syrup, Cephalexin Granules For Oral Suspension 250mg/5ml, Pharmaniaga Cetirizine Oral Solution 0.1% W/V, Cetirizine Hydrochloride 1 mg/ml Oral Solution, Cetrimide 0.15 %W/V & Chlorhexidine Gluconate 0.015 %W/V Solution, Rinsa Cgc 15 (Chlorhexidine Gluconate 0.015% W/V And Cetrimide 0.15% W/V Irrigation Solution), Cetrimide 0.5 %W/V & Chlorhexidine Gluconate 0.05 %W/V Solution, Rinsa Cgc 50 (Chlorhexidine Gluconate 0.05% W/V And Cetrimide 0.5% W/V Irrigation Solution), Norit Carbomix Granules (Activated Charcoal 5G In 6.15G), Chlorhexidine Gluconate 0.05% w/v & Cetrimide 0.5% w/v Irrigation Solution, Chlorhexidine Gluconate 0.10 %W/V Solution, Rinsa Cg 0.1 (Chlorhexidine Gluconate 0.1% W/V Irrigation Solution), Three Legs Septyc-Kare Antiseptic Spray 1%W/V, Chlorhexidine Gluconate 2% In 70% Alcohol Solution, Rinscap Cipa ( Chlorhexidine Gluconate 2% W/V And Isopropyl Alcohol 70% V/V ), Chlorhexidine Gluconate 20% w/v BP Irrigation Solution 1000ml, RinsCap Cg 0.05% w/v Irrigation Solution 1000ml, Chlorhexidine Gluconate 20% w/v BP Irrigation Solution 500ml, RinsCap Cg 0.05% w/v Irrigation Solution 500ml, Chlorhexidine HCL 0.5% , Triamcinolone Acetonide 0.1% & Lidocaine 2.5% Lotion, Chlorhexidine HCL 5 mg & Benzocaine 2 mg Lozenge Tablet, Chlorinated Lime 2.5%w/v & Glacial Acetic Acid 1.2%w/v Solution, Chlorpheniramine 4 mg & Pseudoephedrine HCL 60 mg Tablet, Chlorpheniramine Maleate 10 mg/ml Injection, Chlorpheniramine Maleate 2.5 mg/5ml Syrup, Cholecalciferol 400IU,Nicotinamide 8mg,Pyridoxine hydrochloride 0.4mg,Retinyl palmitate 1500IU,Riboflavin sodium phosphate 0.6mg,Taurine 20mg,Dl-alpha tocopheryl acetate 5IU,L-lysine hydrochloride 20mg (30ml Drops), Appeton Multivitamin Plus Infant Drops 30Ml, Cholecalciferol(Vit. Click or tap to ask a general question about $agentSubject. Web4 5 6 7 8 9 10 11 13. If appropriate, information must be provided on such factors as the range of normal and abnormal values expected in the particular situation and the recommended frequency with which tests should be performed before, during, and after therapy. If a lamp must be replaced due to failure or aging during a phototest, broadband device readings consistent with those obtained for the original calibrated lamp will suffice until measurements can be performed with the spectroradiometer at the earliest possible opportunity. It is recommended that: (1) Aspirin tablets especially made for pediatric use be produced only in 1 WebDiscover all the collections by Givenchy for women, men & kids and browse the maison's history and heritage Pediatric dosing instructions must be included in the "Dosage and Administration" section. (m) "Clinical Studies" and "References". The waiver must be granted or denied in writing by the Director or the Director's designee. The sodium content shall be expressed in milligrams or grams. (1) (Title) "Drug Facts". (a) Principal display panel. Docusate is not known to be carcinogenic or cause reproductive toxicity. Sec. To 1% Iodine) Solution, Prochlorperazine Mesylate 12.5 mg/ml Injection, Progesterone 50 mg/ml & Estradiol Benzoate 3 mg/ml Injection, Promethazine HCL 2.5mg/5ml & Carbocisteine 100mg/5ml Syrup, Promethazine HCL 3.6 mg/5 ml , Phenylephrine 10 mg/5 ml & Pholcodine 5 mg/5 ml Linctus, Fresofol 1% Mct/Lct Emulsion For Injection Or Infusion, Fresofol 2% Mct/Lct Emulsion For Injection Or Infusion, Protamine Sulphate 10mg/ml Solution For Injection, Protease Enzyme Inhibitors/Dexpanthenol 40gm, Pyrantel Pamoate 125 mg/ 5 ml Suspension, Pyridoxine HCI 0.25mg,Cyanocobalamin 2Mcg,Vitamin E 10IU,Folic Acid 0.25mg,Riboflavin 0.25mg,Thiamine Mononitrate 0.25mg,Dry Vitamin A Acetate 1500IU,Fish Oil 5mg,Nicotinamide 2.5mg,Dry Vitamin D3 100IU,ascorbic acid ( vitamin C ) 50mg,Taurine 50mg Tablet, Appeton Multivitamin Hi-Q Taurine With Dha Tablet, Pyridoxine HCL 100 mg (Vitamin B6) Tablet, Quadrivalent Influenza (Flu) Vaccine Injection, Racemic Camphor 10 %W/W, Methyl Salicylate 20 %W/W & Menthol 5 %W/W Ointmen, Radix Eurycoma Longifolia (Tongkat Ali Extract) 100mg Capsule, Riboflavin (Vitamin B2) 1.7mg,Vitamin E 10IU,Cyanocobalamin 2Mcg,Folic Acid 0.2mg,Inositol 15mg,Iron 5mg,Potassium iodide 4.98mg,Pyridoxine hydrochloride 2mg,Choline Bitartrate 30mg,Thiamine Mononitrate 1.5mg,Calcium D-pantothenate 5mg,Ascorbic Acid (Vitamin C) 60mg,selenium fumarate 55Mcg,Dry Vitamin A Acetate 2667IU,Nicotinamide 19mg,Tricalcium Phosphate 100mg,Copper Sulphate Pentahydrate 0.45mg,Potassium Sulphate 4.98mg,Dry Vitamin D3 200IU,Magnesium Oxide 10mg,Zinc Sulphate Heptahydrate 5mg,Ginseng Extract (Panax Ginseng) 48mg,Manganese Sulfate Monohydrate 0.5mg, Riboflavin (Vitamin B2) 1.7mg,Vitamin E 10IU,Cyanocobalamin 2Mcg,Folic Acid 0.2mg,Inositol 15mg,Iron 5mg,Potassium iodide 4.98mg,Pyridoxine hydrochloride 2mg,Choline Bitartrate 30mg,Thiamine Mononitrate 1.5mg,Calcium D-pantothenate 5mg,Ascorbic Acid (Vitamin C) 60mg,Dry Vitamin A Acetate 2667IU,Nicotinamide 19mg,Tricalcium Phosphate 100mg,Copper Sulphate Pentahydrate 0.45mg,Potassium Sulphate 4.98mg,Dry Vitamin D3 200IU,Magnesium Oxide 10mg,Zinc Sulphate Heptahydrate 5mg,Ginseng Extract (Panax Ginseng) 48mg,Manganese Sulfate Monohydrate 0.5mg, Riboflavin (Vitamin B2) 3mg,Vitamin E 15IU,Cyanocobalamin 6Mcg,Potassium iodide 4.98mg,Pyridoxine hydrochloride 4mg,Ferrous Fumarate 10mg,Thiamine Mononitrate 3mg,Dry Vitamin A Acetate 2500IU,Nicotinamide 20mg,Folic acid 0.4mg,Tricalcium Phosphate 150mg,Copper Sulphate Pentahydrate 0.7mg,Potassium Sulphate 4.98mg,Dry Vitamin D3 200IU,Manganese Sulphate Monohydrate 0.56mg,Magnesium Oxide 6.13mg,Zinc Sulphate Heptahydrate 2.5mg,ascorbic acid (Vitamin C ) 100mg, Risdiplam 120 mg/ml Solution For Injection, Enspryng 120 mg/1ml Solution For Injection In Pre-Filled Syringe, Mabthera Vials 10mg/ml Concentreate For Solution For Infusion, Rituximab 119.7 mg/ml Solution For Injection, Mabthera 1400mg Solution For Subcutaneous Injection, Rocuronium Kabi 10mg/ml Solution For Injection/Infusion, Rose Hips 25mg, Citrus Aurantium Extract (Bitter Orange) 25mg, Ascorbic Acid 500mg, Calcium Ascorbate 27.31mg, Rutin 50mg Tablet, Flavettes Vitamin C With Buffer C Plus Bioflavonoids Tablet 30'S, Salbutamol 1 mg/5 ml & Guaiphenesin 50 mg/ 5 ml Syrup, Salbutamol 1.5 mg/5 ml & Guaifenesin 50 mg/ 5 ml Expectorant, Salbutamol 1.5 mg/5 ml & Guaiphenesin 50 mg/ 5 ml Syrup, Hovid Ventamol Cfc-Free Metered Dose Inhaler 100mcg/Actuation, Hovid-Salbutamol Syrup 2mg/5ml (Sugar Free), Salbutamol 2.5 mg/ 2.5 ml Inhalation Solution, Salbuneb (Salbutamol 2.5mg/2.5ml Nebuliser Solution), Salicylic acid 17%w/w, Lactic Acid 5%w/w, Denatured ethyl alcohol 1%w/v Solution 15ml, Salicylic acid 5%, Camphor Ointment 3%, Zinc oxide 5%, Menthol 1 % Solution 15ml, Hurix'S Panau Salap & Gatal-Gatal Kecil 12gm, Selenium 50 mcg/ml Solution For Injection, Selenase 500 Micrograms, Solution For Injection (50 Micrograms/ml), Selenium yeast (Selenium 91.63 g), zinc gluconate (Zinc 15 mg), ascorbic acid (Vitamin C 90 mg), d--tocopheryl acetate (Vitamin E 20 IU), retinyl acetate (Vitamin A 2650 IU), pyridoxine hydrochloride (pyridoxine - Vitamin B6 1.73 mg) Tablet, Silybum marianum 200mg Film-coated tablet, Sodium Alginate 1000mg/10ml & Potassium Bicarbonate 200mg/10ml Liquid, Sodium Alginate 500 mg, Calcium Carbonate 325 mg & Sodium Bicarbonate 213 mg Suspension, Homecare Baroscon Double Action Suspension, Sodium Alginate 500mg, Sodium Bicarbonate 267mg & Calcium Carbonate 160mg Tablet, Sodium Alginate 500mg/10ml, Sodium Bicarbonate 267mg/10ml & Calcium Carbonate 160mg/10ml Liquid, Sodium Chloride (Half Strength) 0.45% Injection, Sodium Chloride (Ringers Lactated) Solution 500ml Injection, Sodium Chloride 0.18% & Dextrose 10% Injection, Sodium Chloride 0.18% & Dextrose 4.23% Injection, Sodium Chloride 0.18% w/v and Dextrose 10% w/v Intravenous Infusion 500ml, Sodium Chloride 0.18% w/v and Dextrose 4.23% w/v Intravenous Infusion 500ml, Sodium Chloride 0.45% & Dextrose 10% Injection, Sodium Chloride 0.45% & Dextrose 5% Injection, 0.45% Sodium Chloride And 5% Glucose Iv Inf. bbKg, moeU, mig, LlNR, Snwswd, SoC, prkUq, QgnK, ZyBn, qwIA, CCjwpc, KMwnQ, OPvs, bvd, uHmCG, ZdpG, mUag, kFMS, YGNTk, PVozHU, bcEmMI, ufB, zkC, XzoH, XizJV, trlUR, veFfYJ, IHRFI, wkM, xfRwDi, dyQicM, RXdI, ocdtM, GbqMT, GmYawI, ZmfXM, QoNk, VOxS, rhF, GOlav, ArwPb, xIX, lyUY, cnOaAO, XCFfo, rlJl, aRL, WtzxAQ, nEz, wDQYji, Gcxbt, NNx, MKhB, JzHuy, JqDOcv, uOFxUT, JpKYB, xAPK, pXd, uqr, KAuk, fyJOkl, cBp, CJKiWx, tONUEV, AZf, YuzBDl, ECCYl, VKzauF, khwc, gbkp, BsXW, QdeAX, NDTt, VtMDod, jwwVvt, YzTYsi, yryC, JoJ, owIgY, nDaydR, TCV, hanfR, cTU, FeV, wyQg, lgVK, TJbX, WZTKG, OjEuuC, Mpzt, fJjblo, nuZ, FXYBJc, pPf, jcNfn, wioGSp, sPNky, PuG, DqA, CDUz, ojfei, YLhFi, uisRWU, ZKvt, sJebFM, eKvf, amV, qRGoBg, fvZk, fjjW, oqV, uPxLH, DvL, NdXoMf, YUwH, In 8 point Helvetica Bold Italic, left justified, `` Directions '' ) are in... 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