Label: EVES CENTELLA 20 V1 VOLUME AMPOULE- centella asiatica liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 83113-0001-1 - Packager: eveskorea
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 21, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EVES CENTELLA 20 V1 VOLUME AMPOULE
centella asiatica liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83113-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CENTELLA ASIATICA (UNII: 7M867G6T1U) (CENTELLA ASIATICA - UNII:7M867G6T1U) CENTELLA ASIATICA 1 g in 100 mL Inactive Ingredients Ingredient Name Strength SUCRALFATE (UNII: XX73205DH5) GLUTATHIONE (UNII: GAN16C9B8O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83113-0001-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/22/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/22/2022 Labeler - eveskorea (693718792) Registrant - eveskorea (693718792) Establishment Name Address ID/FEI Business Operations eveskorea 693718792 manufacture(83113-0001)