Label: ORGANIC NIGHT REPAIR AMPOULE- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69142-020-01, 69142-020-02 - Packager: yeojaya
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 17, 2018
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Aloe Barbadensis Leaf Water, Sodium Hyaluronate, Butylene Glycol, Glycerin, Palmitoyl Pentapeptide-4, Glyceryl Glucoside, 1,2-Hexanediol, rh-Oligopeptide-1, Trehalose, Polysorbate 20, Sorbitol, Arginine, Petroselinum Sativum (Parsley) Extract, Cucumis Sativus (Cucumber) Fruit Extract, Althaea Officinalis Root Extract, Centaurea Cyanus Flower Extract, Citrus Limon (Lemon) Fruit Extract, Red Ginseng Extract, Calendula Officinalis Flower Extract, Caprylyl Glycol, Illicium Verum (Anise) Fruit Extract, Pearl Powder, Fragrance, Ceramide NP
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ORGANIC NIGHT REPAIR AMPOULE
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69142-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.12 g in 45 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 g in 45 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69142-020-02 1 in 1 CARTON 08/01/2018 1 NDC:69142-020-01 45 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2018 Labeler - yeojaya (688735127) Registrant - yeojaya (688735127) Establishment Name Address ID/FEI Business Operations yeojaya 688735127 manufacture(69142-020)