Label: QYO QYO TANGERINE BRIGHT MOIST MASK PACK- allantoin cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 71733-106-01 - Packager: LaLa Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 1, 2019
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
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive Ingredients
Water, Glycerin, Propanediol, 1,2-Hexanediol, Butylene Glycol, Sodium Polyacrylate, Portulaca Oleracea Extract, Hydroxyethyl Urea, Arginine, Panthenol, Acetyl Glucosamine, Pantolactone, Centella Asiatica Extract, Disodium EDTA, Sodium Hyaluronate, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Phenoxyethanol, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Beta-Glucan, Citrus Unshiu Peel Extract, Ethylhexylglycerin, Fragrance
- Other Information
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL Qyo Qyo Tangerine Bright + Moist Mask Pack 23mL
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INGREDIENTS AND APPEARANCE
QYO QYO TANGERINE BRIGHT MOIST MASK PACK
allantoin clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71733-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.2 g in 23 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TANGERINE PEEL (UNII: JU3D414057) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71733-106-01 1 in 1 PACKAGE 01/01/2018 1 23 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/01/2018 Labeler - LaLa Co., Ltd. (694617781) Establishment Name Address ID/FEI Business Operations LaLa Co., Ltd. 694617781 manufacture(71733-106)