Label: QYO QYO TANGERINE BRIGHT MOIST JELLY SUNBLOCK SPF 40- octinoxate, titanium dioxide, zinc oxide gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71733-100-01 - Packager: LaLa Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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, 2018
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
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
- Apply liberally 15 minutes before sun exposure and as needed.
- Reapply as needed or after towel drying, swimming, or sweating.
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 a.m. to 2 p.m.
• Wear long-sleeved shirts, pants, hats, and sunglasses- Children under 6 months: Ask a doctor
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Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Glycerin, Dipropy- lene Glycol, Butylene Glycol, Betaine, Polyoxyethylene Hydrogenated Castor Oil, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Camelia Sinensis (Green Tea) Leaf Extract, Collagen, Hyaluronic Acid, Morus Alba Bark Extract, Citrus Unshiu Peel Extract, 1-2-Hexanediol, Tocopheryl Acetate, Carbomer, Triethanolamine, Allantoin, Disodium EDTA, Fragrance, FD&C Yellow No. 5 (Cl 19140)
- Other Information
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL Qyo Qyo Tangerine Bright + Moist Jelly Sunblock SPF 40 from jeju
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INGREDIENTS AND APPEARANCE
QYO QYO TANGERINE BRIGHT MOIST JELLY SUNBLOCK SPF 40
octinoxate, titanium dioxide, zinc oxide gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71733-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 2.5 g in 50 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 1 g in 50 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.5 g in 50 mL Inactive Ingredients Ingredient Name Strength DIPROPYLENE GLYCOL (UNII: E107L85C40) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) TANGERINE PEEL (UNII: JU3D414057) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYALURONIC ACID (UNII: S270N0TRQY) MORUS ALBA BARK (UNII: 7O71A48NDP) WATER (UNII: 059QF0KO0R) BETAINE (UNII: 3SCV180C9W) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) TOCOPHEROL (UNII: R0ZB2556P8) CARBOMER 940 (UNII: 4Q93RCW27E) ALLANTOIN (UNII: 344S277G0Z) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71733-100-01 1 in 1 BOX 01/01/2018 1 50 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/01/2018 Labeler - LaLa Co., Ltd. (694617781) Establishment Name Address ID/FEI Business Operations LaLa Co., Ltd. 694617781 manufacture(71733-100)
