Label: DAILY PREVENTION PURE MINERAL HYDRATING MOISTURIZER SPF30- zinc oxide cream
- NDC Code(s): 62742-4245-1, 62742-4245-2, 62742-4245-3, 62742-4245-4
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 22, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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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 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
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Water /Aqua/Eau, Cyclopentasiloxane, Dicaprylyl Carbonate, Polyhydroxystearic Acid, Dimethicone, Glycerin, Lecithin, Isohexadecane, Aloe Barbadensis Leaf Juice, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Dimethicone/PEG-10/15 Crosspolymer, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Magnesium Sulfate Heptahydrate, Acetyl Zingerone, Phenoxyethanol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Squalane, Phosphatidylcholine, Mannitol, Vanilla Planifolia Fruit Extract, Camellia Sinensis Leaf Extract, Methyl Propanediol, Sodium Hyaluronate, Polysorbate 60,Ectoin,Sodium Citrate,Sorbitan Isostearate, Tocopherol, Stearic Acid, Palmitic Acid, Haematococcus Pluvialis Extract, Tetrahexyldecyl Ascorbate, Panthenol, Phenylpropanol, Sodium Benzoate, Potassium Sorbate
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY PREVENTION PURE MINERAL HYDRATING MOISTURIZER SPF30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4245 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 18.1 g in 100 g Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ISOHEXADECANE (UNII: 918X1OUF1E) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) PALMITIC ACID (UNII: 2V16EO95H1) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) ACETYL ZINGERONE (UNII: V9D92S9YE5) HEXYLENE GLYCOL (UNII: KEH0A3F75J) MANNITOL (UNII: 3OWL53L36A) VANILLA (UNII: Q74T35078H) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ALOE VERA LEAF (UNII: ZY81Z83H0X) HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472) PHENYLPROPANOL (UNII: 0F897O3O4M) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE (UNII: 1Q73Q2JULR) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) METHYLPROPANEDIOL (UNII: N8F53B3R4R) PANTHENOL (UNII: WV9CM0O67Z) SQUALANE (UNII: GW89575KF9) PHOSPHATIDYLCHOLINE TRANSLOCATOR ABCB4 (UNII: 9EI49ZU76O) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ECTOINE (UNII: 7GXZ3858RY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4245-1 7 g in 1 TUBE; Type 0: Not a Combination Product 02/22/2024 2 NDC:62742-4245-2 142 g in 1 TUBE; Type 0: Not a Combination Product 02/22/2024 3 NDC:62742-4245-4 1 in 1 CARTON 02/22/2024 3 NDC:62742-4245-3 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 02/22/2024 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4245)