Label: TRIPLE CROWN CORDYCEPS SUPER ESSENCE MASK- adenosine patch
-
Contains inactivated NDC Code(s)
NDC Code(s): 81211-050-01, 81211-050-02 - Packager: BIO-S 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 December 15, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
-
Direction
1. Please smooth out the skin after cleansing.
2. Open the mask and take it out, then make sure it is evenly attached to the entire face except for areas around the eyes and the mouth.
3. After 10~20 minutes, gently remove the mask and let the remaining essence be absorbed into your skin by tapping it lightly. - QUESTIONS
-
INACTIVE INGREDIENTS
Water, Glycerin, Methylpropanediol, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Allantoin, Carbomer, Triethanolamine, Disodium EDTA, Fragrance, Cordyceps Sinensis Extract, Panax Ginseng Root Extract, Velvet Extract, Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Morus Alba Bark Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TRIPLE CROWN CORDYCEPS SUPER ESSENCE MASK
adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81211-050 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 25 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Methylpropanediol (UNII: N8F53B3R4R) Phenoxyethanol (UNII: HIE492ZZ3T) PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) Allantoin (UNII: 344S277G0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81211-050-02 10 in 1 CARTON 12/01/2020 1 NDC:81211-050-01 25 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2020 Labeler - BIO-S CO.,LTD (690007651) Registrant - BIO-S CO.,LTD (690007651) Establishment Name Address ID/FEI Business Operations INTAGLIO.INC 690253971 manufacture(81211-050)