Label: LAPCOS SUNTIAGING EYE ZONE COOLING GOLF PAT CH S- niacinamide, adenosine patch
-
Contains inactivated NDC Code(s)
NDC Code(s): 82971-010-01 - Packager: JC FAMILY 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 2, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENTS
Water/Aqua, Glycerin, Dipropylene Glycol, Dipropylene Glycol, Polyacrylic Acid, Agar, Sodium Polyacrylete, Hydrocyacetophenone, Xanthan Gum, Caprylyl Glycol, Cellulose Gum, Disodium EDTA, Tartaric Acid, Cetyl Ethylhexanoate, Caprylyl/Capryl Glucoside, Butylene Glycol, Menthyl Lactate, Aluminum Glycinate, Panthenol, Sodium Hyaluronate, 1,2-Hexanediol, Centella Asiatica Extract, Hydrolyzed Collagen, Dipotassium Glycyrrhizate, Arbutin, Houttuynia Cordata Extract, Alpha-Arbutin, Glutathione, Ascorbic Acid, Madecassoside, Polyglyceryl-10 Laurate,Palmitoyl Pentapeptide-4, Palmitoyl Tripeptide-1, Hexapeptide-9, Aceytl Hexapeptide-8, Tripeptide-1, Copper Tripeptide-1
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
-
Directions
■. Open the product to take out the patch. Remove the protection.
■. Place the patch on the under-eye, cheekbone, cheek and other areas.
■. Leave it for 30 minutes before removing.
■. You can also use it for longer time during outdoor activities. Also suitable to use on top of sunscreen or makeup. The patch may become less adhesive when used on oily skin.
- Other Information
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LAPCOS SUNTIAGING EYE ZONE COOLING GOLF PAT CH S
niacinamide, adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82971-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.02 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.0004 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82971-010-01 4 in 1 CARTON; Type 0: Not a Combination Product 08/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2022 Labeler - JC FAMILY Co., Ltd (688238575) Registrant - JC FAMILY Co., Ltd (688238575) Establishment Name Address ID/FEI Business Operations Kovas Co., Ltd. 688783559 manufacture(82971-010)
