Label: DAILY PREVENTION PURE MINERAL TINTED MOISTURIZER SPF 30- titanium dioxide and zinc oxide cream
- NDC Code(s): 62742-4254-1, 62742-4254-2, 62742-4254-3
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 15, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
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DOSAGE & ADMINISTRATION
Directions • apply generously 15 minutes before sun exposure • children under 6 months of age: Ask a doctor • reapply: • after 40 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.
- KEEP OUT OF REACH OF CHILDREN
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients: Agua/Water/Eau, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Dimethicone, Glycerin, Cyclohexasiloxane, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Dimethicone /PEG-10/15 Crosspolymer, Aluminum Hydroxide, Stearic Acid, Sodium Chloride, Cetearyl Olivate, Acetyl Zingerone, PolyglyceryI-4 lsostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Dimethicone/Polyglycerin-3 Crosspolymer, Phenoxyethanol, Sorbitan Oliveto, Caprylic/Capric Triglyceride, Triethoxysilyethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Dimethicone/Vinyl Dimethicone Crosspolymer, Tocopheryl Acetate, Phosphatidylcholine, Mannitol, Vanilla Planifolia Fruit Extract, Camellia Sinensis Leaf Extract, Dipropylene Glycol, Benzoic Acid, Methyl Propanediol, Triethoxycapryiyisilane, Sodium Citrate, Ectoin, Stearic Acid, Palmitic Acid, Haematococcus Pluvialis Extract, Tocopherol, Tatrahexyldecyl Ascorbate, Panthenol, Phenylpropanol, Alumina, Magnesium Oxide, Sodium Benzoate, Potassium Sorbate, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Sodium Ferrocyanide, CI 77891, CI 77499, CI 77492, CI 77491.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY PREVENTION PURE MINERAL TINTED MOISTURIZER SPF 30
titanium dioxide and zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4254 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.7 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 6 g in 100 g Inactive Ingredients Ingredient Name Strength ACETYL ZINGERONE (UNII: V9D92S9YE5) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) SORBITAN OLIVATE (UNII: MDL271E3GR) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) TOCOPHEROL (UNII: R0ZB2556P8) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CYCLOMETHICONE 6 (UNII: XHK3U310BA) BENZOIC ACID (UNII: 8SKN0B0MIM) PHENYLPROPANOL (UNII: 0F897O3O4M) MAGNESIUM OXIDE (UNII: 3A3U0GI71G) SODIUM FERROCYANIDE (UNII: 5HT6X21AID) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM CHLORIDE (UNII: 451W47IQ8X) WATER (UNII: 059QF0KO0R) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA) HEXYL LAURATE (UNII: 4CG9F9W01Q) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GREEN TEA LEAF (UNII: W2ZU1RY8B0) DIPROPYLENE GLYCOL (UNII: E107L85C40) MANNITOL (UNII: 3OWL53L36A) METHYLPROPANEDIOL (UNII: N8F53B3R4R) ECTOINE (UNII: 7GXZ3858RY) PALMITIC ACID (UNII: 2V16EO95H1) FERRIC OXIDE RED (UNII: 1K09F3G675) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) SODIUM CITRATE (UNII: 1Q73Q2JULR) HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472) ALUMINUM OXIDE (UNII: LMI26O6933) HEXYLENE GLYCOL (UNII: KEH0A3F75J) STEARIC ACID (UNII: 4ELV7Z65AP) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) PANTHENOL (UNII: WV9CM0O67Z) VANILLA (UNII: Q74T35078H) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SODIUM BENZOATE (UNII: OJ245FE5EU) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) PHOSPHATIDYLCHOLINE TRANSLOCATOR ABCB4 (UNII: 9EI49ZU76O) DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER (UNII: 2P2G24V6T9) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4254-1 7 g in 1 TUBE; Type 0: Not a Combination Product 03/15/2024 2 NDC:62742-4254-3 1 in 1 CARTON 03/15/2024 2 NDC:62742-4254-2 73 g 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 Drug M020 03/15/2024 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4254)
