Label: RE CELL CURE AMPOULE- adenosine, niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82665-0002-1, 82665-0002-2 - Packager: Dermabqcell Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated October 8, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Propylene Glycol, Glycerin, Niacinamide, Butylene Glycol, Polysorbate 20,
Scutellaria Baicalensis Root Extract, Paeonia Suffruticosa Root Extract, Allantoin,
1,2-Hexanediol, Hydroxyethylcellulose, Arabidopsis Thaliana Extract, Lecithin,
Poloxamer407, Arginine, Adenosine, Disodium EDTA, Sodium Hyaluronate,
Lavandula Angustifolia (Lavender) Oil, Human Adipocyte Conditioned Media Extract,
Centella Asiatica Extract, Houttuynia Cordata Extract, Pinus Densiflora Extract,
Eucalyptus Globulus Leaf Extract, Vitis Vinifera (Grape) Seed Extract,
Ethylhexylglycerin, rh-Oligopeptide-1, Diospyros Kaki Leaf Extract, Cinnamomum
Cassia Bark Extract, Artemisia Princeps Leaf Extract, Chrysanthellum Indicum
Extract, Chaenomeles Sinensis Fruit Extract, Camellia Sinensis Leaf Extract, Punica
Granatum Fruit Extract, Ficus Carica (Fig) Fruit Extract, Morus Alba Fruit Extract,
Ginkgo Biloba Nut Extract - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RE CELL CURE AMPOULE
adenosine, niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82665-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 2 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82665-0002-2 10 in 1 PACKAGE 10/08/2022 1 NDC:82665-0002-1 2 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 unapproved drug other 10/08/2022 Labeler - Dermabqcell Co., Ltd. (695556088) Registrant - Dermabqcell Co., Ltd. (695556088) Establishment Name Address ID/FEI Business Operations Dermabqcell Co., Ltd. 695556088 label(82665-0002) Establishment Name Address ID/FEI Business Operations Rainbow Beauty Cosmetic Co Ltd 695684820 manufacture(82665-0002)
