Label: PRESTIGE SHINY GOLD- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69628-020-01, 69628-020-02 - Packager: Maywell 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 September 19, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Bifida Ferment Filtrate, Glycerin, Butylene Glycol, Water, Methyl Gluceth-20, Carbomer, PEG-14M, 1,2-Hexanediol, Polysorbate 80, Caprylyl Glycol, Allantoin, Sodium Hydroxide, Gold, Fragrance, Sodium Hyaluronate, Phenoxyethanol, Illicium Verum (Anise) Fruit Extract, Aloe Barbadensis Leaf Extract, Ethylhexylglycerin, Propanediol, Sodium Hyaluronate Crosspolymer, Hydrolyzed Glycosaminoglycans, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Mentha Viridis (Spearmint) Extract, Monarda Didyma Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Origanum Vulgare Leaf Extract, Orchid Extract, Benzyl Glycol, Hydrolyzed Hyaluronic Acid, Hyaluronic Acid, Raspberry Ketone
- PURPOSE
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WARNINGS
Warnings:
For external use only
1. In case of having side effects such as red rash, swollenness and/or itching while using this cosmetic, or in case such symptoms appear by direct sunlight after using it, consult a dermatologist immediately.
2. Do not apply it on the part where you have a scar, eczema or dermatitis.
3. Precautions for treatment and storage.
1) Keep it out of the reach of children.
2) Avoid the place where the direct sunlight is.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PRESTIGE SHINY GOLD
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69628-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.60 g in 30 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 30 g 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:69628-020-02 1 in 1 CARTON 08/01/2018 1 NDC:69628-020-01 30 g 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 - Maywell Co,. Ltd. (689512503) Registrant - Maywell Co,. Ltd. (689512503) Establishment Name Address ID/FEI Business Operations Interkos Co.,Ltd. 689850314 manufacture(69628-020)
