Label: BLANCHET GLAM PEARL RADIANCE CAPSUL E SERUM- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 79171-030-01, 79171-030-02 - Packager: Hanmi International Corp.
- 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 August 6, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- Uses
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Directions
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INACTIVE INGREDIENTS
Water,Dipropylene Glycol,1,2-Hexanediol,Agar,Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Synthetic Fluorphlogopite,Titanium Dioxide(CI 77891),Polyglyceryl-10Laurate,Polyglyceryl-10Stearate, Ethylhexylglycerin,Hydrolyzed Pearl,Ocimum Basilicum (Basil) Oil, Elettaria Cardamomum Seed Oil,Pelargonium Graveolens Flower Oil, Lavandula Angustifolia (Lavender) Oil,Citrus Aurantium Dulcis (Orange) Flower Oil,Olea Europaea (Olive) Fruit Oil,Pogostemon Cablin Oil, Rosa Damascena Flower Oil,Rosmarinus Officinalis (Rosemary) Leaf Oil, Santalum Album (Sandalwood) Oil,Water,Glycerin,Propanediol, Hydroxyacetophenone,1,2-Hexanediol ,Centella Asiatica Extract,Butylene Glycol,Propanediol ,Portulaca Oleracea Extract,1,2-Hexanediol, Centella Asiatica Extract,1,2-Hexanediol ,Panax Ginseng Leaf/Stem Extract,
Moringa Oleifera Leaf Extract,1,2-Hexanediol , Hydrolyzed corn starch, Beta vulgaris (Beet) Root Extract,Glycerin,Bifida Ferment Lysate,
Glutathione,Plankton extract,Disodium EDTA,Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Xanthan Gum - PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BLANCHET GLAM PEARL RADIANCE CAPSUL E SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79171-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.8 g in 40 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 40 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Dipropylene Glycol (UNII: E107L85C40) 1,2-Hexanediol (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79171-030-02 1 in 1 CARTON 08/01/2020 1 NDC:79171-030-01 40 mL in 1 BOTTLE; 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(79171-030)
