Label: BLANCHET GLAM PEARL RADIANCE AMPOULE- niacinamide, adenosine lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 79171-010-01, 79171-010-02 - Packager: Hanmi International Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 6, 2020
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- ACTIVE INGREDIENTS
- PURPOSE
- Uses
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Directions
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INACTIVE INGREDIENT
Water, Glycerin, Caprylyl Methicone, 1,2-Hexanediol, Cetyl Ethylhexanoate, Betaine, Pentylene Glycol, Phenyl Trimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl, Taurate Copolymer, Hydroxyacetophenone, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Xanthan Gum, Hydrolyzed Pearl, Olea Europaea (Olive) Fruit Oil, Disodium EDTA, Pelargonium Graveolens Flower Oil, Hydrolyzed Hibiscus Esculentus Extract, Lupinus Albus Seed Extract, Moringa Oleifera Seed Extract, Santalum Album (Sandalwood) Oil, Citrus Aurantium Dulcis (Orange) Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Pogostemon Cablin Oil, Lavandula Angustifolia (Lavender) Oil, Rosa Damascena Flower Oil, Ocimum Basilicum (Basil) Oil, Elettaria Cardamomum Seed Oil, Butylene Glycol, Glutathione, Polymethylsilsesquioxane, Avena Sativa (Oat) Kernel Extract, Diospyros Kaki Leaf Extract, Angelica Keiskei Leaf/Stem Extract, Camellia Sinensis Leaf Extract, Portulaca Oleracea Extract, Diamond powder
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLANCHET GLAM PEARL RADIANCE AMPOULE
niacinamide, adenosine lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79171-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.60 g in 80 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.03 g in 80 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79171-010-02 1 in 1 CARTON 08/01/2020 1 NDC:79171-010-01 80 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2020 Labeler - Hanmi International Corp. (557807637) Registrant - Hanmi International Corp. (557807637) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(79171-010)