Label: QYO QYO TANGERINE BRIGHT MOIST- allantoin, dimethicone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 71733-103-01 - 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, Butylene Glycol, C12-15 Alkyl Benzoate, Glycerin, Caprylic/ Capric Triglyceride, 1,2-Hexanediol, Macadamia Ternifolia Seed Oil, Cetyl Alcohol,Polysorbate 60, Stearyl Dimethicone, Stearic Acid, Caprylyl Glycol, Chlorphenesin, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Cetearyl Alcohol, Sorbitan Sesquioleate, Tocopheryl Acetate, Isohexadecane, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Arginine, Octadecene, Citrus Unshiu Peel Extract, Rosa Centifolia Flower Water, Polysorbate 80, Disodium EDTA, Ethylhexylglycerin, Dipotassium Glycyrrhizate, Xanthan Gum, Glyceryl Stearate, Iris Ensata Extract, Cosmos Sulphureus Flower/ Leaf/Stem Extract, Lilium Candidum Flower Extract, Rosa Centifolia Flower Extract, Jasminum Officinale (Jasmine) Flower Extract, Hibiscus Rosa-Sinensis Flower/Leaf Extract, Nelumbo Nucifera Flower Extract, Phenoxyethanol, Beta-Carotene, Citric Acid, Tocopherol, Fragrance, FD&C Yellow No. 6 (CI 15985)
- Other Information
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL Qyo Qyo Tangerine Bright + Moist Lotion 120mL
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INGREDIENTS AND APPEARANCE
QYO QYO TANGERINE BRIGHT MOIST
allantoin, dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71733-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.5 g in 120 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.1 g in 120 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TANGERINE PEEL (UNII: JU3D414057) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71733-103-01 1 in 1 BOX 01/01/2018 1 120 mL in 1 BOTTLE, PLASTIC; 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(71733-103)