Label: DAILY PREVENTION SHEER MATTE MOISTURIZER SPF30- homosalate and octisalate and zinc oxide cream
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NDC Code(s):
62742-4253-1,
62742-4253-2,
62742-4253-3,
62742-4253-4, view more62742-4253-5
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 15, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 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
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients: Aqua/water/Eau, Cyclopentasiloxane, Polyhydroxystearic Acid, Dimethicone, Coconut Alkanes, Stearic Acid, Lecithin, Aloe Barbadensis Leaf Juice, Isohexadecane, lsododecane, Magnesium Sulfate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Polysillcone-11, Coco-Caprylate/Caprate, Dimethicone/PEG-10/15 Crosspolymer, Dipropylene Glycol, Sodium Citrate, Tocopherol, Cetearyl Olivate, Sorbitan Olivate, Sodium Hyaluronate, Phenoxyethanol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Squalane, Polysorbate 60, Sorbitan Isostearate, Caprylyl Glycol, Ethylhexylycerin, Hexylene Glycol, Phosphatidylcholine, Mannitol, Glycerin, Methylpropanediol, Caprylic/Capric Triglyceride, Ectoine, Palmitic Acid, Haematococcus Pluvialis Extract, Tetrahexyldecyl Ascorbate, Panthenol, Phenylpropanol, Vanilla Planifolia Fruit Extract, Silica, Dimethicone/Vinyl Dimethicone Crosspolymer, Acetyl Zingerone, Camellia Sinensis Leaf Extract, Sodium Benzoate, Potassium Sorbate, Octyldodecanol, Sorbitan Oleate, CI 77491, CI 77492
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY PREVENTION SHEER MATTE MOISTURIZER SPF30
homosalate and octisalate and zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4253 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 5 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 9.3 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) MANNITOL (UNII: 3OWL53L36A) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) OCTYLDODECANOL (UNII: 461N1O614Y) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) WATER (UNII: 059QF0KO0R) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) METHYLPROPANEDIOL (UNII: N8F53B3R4R) ECTOINE (UNII: 7GXZ3858RY) PALMITIC ACID (UNII: 2V16EO95H1) PANTHENOL (UNII: WV9CM0O67Z) GREEN TEA LEAF (UNII: W2ZU1RY8B0) DIPROPYLENE GLYCOL (UNII: E107L85C40) ISODODECANE (UNII: A8289P68Y2) SODIUM CITRATE (UNII: 1Q73Q2JULR) TOCOPHEROL (UNII: R0ZB2556P8) CETEARYL OLIVATE (UNII: 58B69Q84JO) SORBITAN OLIVATE (UNII: MDL271E3GR) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) PHOSPHATIDYLCHOLINE TRANSLOCATOR ABCB4 (UNII: 9EI49ZU76O) HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472) VANILLA (UNII: Q74T35078H) FERRIC OXIDE RED (UNII: 1K09F3G675) SQUALANE (UNII: GW89575KF9) ACETYL ZINGERONE (UNII: V9D92S9YE5) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ALOE VERA LEAF (UNII: ZY81Z83H0X) ISOHEXADECANE (UNII: 918X1OUF1E) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) POLYSORBATE 60 (UNII: CAL22UVI4M) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DIMETHICONE (UNII: 92RU3N3Y1O) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) COCONUT ALKANES (UNII: 1E5KJY107T) PHENOXYETHANOL (UNII: HIE492ZZ3T) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PHENYLPROPANOL (UNII: 0F897O3O4M) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) STEARIC ACID (UNII: 4ELV7Z65AP) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4253-1 7 g in 1 TUBE; Type 0: Not a Combination Product 03/15/2024 2 NDC:62742-4253-2 28 g in 1 TUBE; Type 0: Not a Combination Product 03/15/2024 3 NDC:62742-4253-4 1 in 1 CARTON 03/15/2024 3 NDC:62742-4253-3 73 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:62742-4253-5 142 g in 1 TUBE; Type 0: Not a Combination Product 03/15/2024 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(62742-4253)
