Label: MORINGA PURIFY WATER- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72255-010-01, 72255-010-02 - Packager: Oneface co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 May 10, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Moringa Oleifera Seed Extract, Glycerin, Cyclopentasiloxane, Cyclohexasiloxane, Butylene Glycol, Methyl Hydrogenated Rosinate, Cetyl PEG/PPG-10/1 Dimethicone, Sodium Hyaluronate, Beta-Glucan, 1,2-Hexanediol, Caprylhydroxamic Acid, Propanediol, Sodium Chloride, Titanium Dioxide, Aluminum Hydroxide, Triethoxycaprylylsilan, Cyclomethicone, PEG-10 Dimethicone, Dimethicone, Dimethicone/Vinyl Dimethicone, Crosspolymer, Fragrance, Water, Caulerpa Lentillifera Extract, Codium Fragile Extract, Donkey Milk, Honey Extract, Goat Milk Extract, Phenoxyethanol, Ethylhexyglycerin, Saccharide Isomerate, Citric Acid, Sodium Citrate, Potassium PCA, Opuntia Ficus Indica Stem Extract
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MORINGA PURIFY WATER
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72255-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2.0 g in 100 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72255-010-02 1 in 1 CARTON 04/01/2018 1 NDC:72255-010-01 100 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 04/01/2018 Labeler - Oneface co., Ltd. (688219085) Registrant - Oneface co., Ltd. (688219085) Establishment Name Address ID/FEI Business Operations Oneface co., Ltd. 688219085 manufacture(72255-010)
