Label: VITAMIN C LIQUID- allantoin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70663-004-01, 70663-004-02 - Packager: MESO SYSTEM S A
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 2, 2017
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- Official Label (Printer Friendly)
- INACTIVE INGREDIENT
- Warnings
- WARNINGS
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USES
For its antioxidants properties helps to neutralize the free radicals, protecting the skin. It helps to prevent and reduce the appearance of wrinklers, combating the signs of ageing. It is used as coadjuvant in the production of collagen and helps to strenghten the skin, providing a younger and brighter look
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USES
For its antioxidants properties helps to neutralize the free radicals, protecting the skin. It helps to prevent and reduce the appearance of wrinklers, combating the signs of ageing. It is used as coadjuvant in the production of collagen and helps to strenghten the skin, providing a younger and brighter look
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- DIRECTIONS
- QUESTIONS OR COMMENTS?
- ACTIVE INGREDIENT
- VITAMIN C LIQUID
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INGREDIENTS AND APPEARANCE
VITAMIN C LIQUID
allantoin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70663-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.1 mg in 1 mL Inactive Ingredients Ingredient Name Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) 12 mg in 1 mL ASCORBIC ACID (UNII: PQ6CK8PD0R) 20 mg in 1 mL WATER (UNII: 059QF0KO0R) 67.9 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70663-004-02 20 in 1 CARTON 12/14/2016 1 NDC:70663-004-01 5 mL in 1 AMPULE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/16/2016 Labeler - MESO SYSTEM S A (768263100) Registrant - Meso System S A (768263100) Establishment Name Address ID/FEI Business Operations Meso System S A 768263100 manufacture(70663-004)
