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

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredients :

    Zinc Oxide 18.1%

  • PURPOSE

    Purpose:

    Sunscreen

  • INDICATIONS & USAGE

    Uses • helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

  • WARNINGS

    Warnings • For external use only

  • DO NOT USE

    Do not use on damaged or broken skin

  • WHEN USING

    When using this product keep out of eyes. Rinse with water to remove.

  • STOP USE

    Stop use and ask a doctor if rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • 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

    Other information • protect the product in this container from excessive heat and direct sun • Due to the presence of botanical ingredients , this product may change in color over time.

  • 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

    DP Pure Mineral hydrating moist SPF30

  • INGREDIENTS AND APPEARANCE
    DAILY PREVENTION PURE MINERAL HYDRATING MOISTURIZER SPF30 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4245
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE18.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4245-17 g in 1 TUBE; Type 0: Not a Combination Product02/22/2024
    2NDC:62742-4245-2142 g in 1 TUBE; Type 0: Not a Combination Product02/22/2024
    3NDC:62742-4245-41 in 1 CARTON02/22/2024
    3NDC:62742-4245-373 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/22/2024
    Labeler - Allure Labs (926831603)
    Registrant - Allure Labs (926831603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allure Labs926831603manufacture(62742-4245)