Label: SHEER DEFENSE TINTED SPF 46- zinc oxide, octinoxate cream
- NDC Code(s): 72957-002-01
- Packager: Private Label Skin Care
- This is a repackaged label.
- Source NDC Code(s): 39765-023
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 18, 2026
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
• Apply liberally on a clean dry face, avoiding delicate eye area 15 minutes before sun exposure • reapply: • after 80 minutes of swimming • or sweating • immediately after towel drying • at least every 2 hours • 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.– 2 p.m • wear long-sleeved shirts pants, hats, and sunglasses • children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
Water/Aqua/Eau, Cyclopentasiloxane, Niacinamide, Oleth-3 Phosphate, Octyldodecyl Neopentanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glycerin, Knot Grass (Polygonum Aviculare) Extract, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Polyisobutene, PEG-7 Trimethylolpropane Coconut Ether, Ethylhexylglycerin, Tocopheryl Acetate, Triethoxycaprylylsilane, Disodium EDTA, Sodium Hyaluronate, Phenoxyethanol, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
SHEER DEFENSE TINTED SPF 46
zinc oxide, octinoxate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72957-002(NDC:39765-023) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 12 g in 100 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) NIACINAMIDE (UNII: 25X51I8RD4) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) GLYCERIN (UNII: PDC6A3C0OX) POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) PEG-7 TRIMETHYLOLPROPANE COCONUT ETHER (UNII: MVJ3AD73GG) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72957-002-01 57 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/27/2020 12/11/2027 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/27/2020 12/11/2027 Labeler - Private Label Skin Care (116996962) Establishment Name Address ID/FEI Business Operations Private Label Skin Care 116996962 relabel(72957-002)
