Label: BANDHA YOU AND FACE SERUM- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 80623-020-01, 80623-020-02 - Packager: DKCOSTECH
- 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 23, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Dendropanax Morbiferus Leaf Extract, Water, Propanediol, Glycerin, 1,2Hexanediol, Butylene Glycol, betaine, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Carbomer, C12-14 Pareth-12, Allantoin , Aloe Barbadensis Leaf Extract, Astragalus Membranaceus Root Extract,
Boswellia Serrata Extract, Melia Azadirachta Leaf Extract, Phyllanthus Emblica Extract, Trifolium Pratense (Clover) Flower Extract, Garcinia Cambogia Fruit Extract, Fragrance, Disodium EDTA, Xanthan Gum, Sodium Hyaluronate - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
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Directions
1. After using the toner in the morning and evening, pump once or twice during the serum stage, then spread evenly from the inside of the face to the outside.
2. Gently sweep from the inside of the cheeks outwards and apply.
3. Massage in a circular motion from the center of your forehead to outwards.
4. Massage along your jawline starting from the center of the chin and going upwards to the back of your ears. - QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BANDHA YOU AND FACE SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80623-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1.0 g in 50 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propanediol (UNII: 5965N8W85T) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80623-020-02 1 in 1 CARTON 09/01/2020 1 NDC:80623-020-01 50 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 09/01/2020 Labeler - DKCOSTECH (695504288) Registrant - DKCOSTECH (695504288) Establishment Name Address ID/FEI Business Operations HANSCOS Co.,Ltd. 688494423 manufacture(80623-020)