Label: SHEER TINT SPF 45- broad spectrum lotion
- NDC Code(s): 68726-269-11, 68726-269-53
- Packager: CP Skin Health Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 14, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Uses
- Warnings
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Directions
Apply liberally 15 minutes before sun exposure
Reapply:
-after 80 minutes of swimming or sweating
-immediately after towel drying
-at least every 2 hours
Children under 6 montha: ask a doctor
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 skin protecting measures including:
-limit time in the sun, especially from 10 a.m. - 2 p.m.
-wear long-sleeved shirts, pants, hats, and sunglasses.
- Other Information
- Questions?
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Inactive Ingredients
Alumina
Butyloctyl Salicylate
C12-15 Alkyl Benzoate
Caprylyl Glycol
Dimethicone
Dimethicone/PEG-10/15 Crosspolymer
Dimethicone/Vinyl Dimethicone Crosspolymer
Ethylhexylglycerin
Hexylene Glycol
Hydrogen Dimethicone
Iron Oxides
Isododecane
Jojoba Esters
Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer
Octyldodecanol
PEG-9 Polydimethylsiloxyethyl Dimethicone
Phenoxyethanol
Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone
Polymethylsilsesquioxane
Sodium Chloride
Triethoxycaprylylsilane
Trihydroxystearin
Water
- Sheet Tint
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INGREDIENTS AND APPEARANCE
SHEER TINT SPF 45
broad spectrum lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68726-269 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 8.1 g in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 8 g in 100 mL Inactive Ingredients Ingredient Name Strength TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SODIUM CHLORIDE (UNII: 451W47IQ8X) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) ALUMINUM OXIDE (UNII: LMI26O6933) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) OCTYLDODECANOL (UNII: 461N1O614Y) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) ISODODECANE (UNII: A8289P68Y2) PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68726-269-11 177 mL in 1 CAN; Type 0: Not a Combination Product 05/01/2020 2 NDC:68726-269-53 192 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2020 Labeler - CP Skin Health Group, Inc. (611921669)
