Label: WALGREENS DARK TANNING OIL SUNSCREEN SPF 4- octinoxate spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 12/12

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

  • Active ingredient

    Octinoxate 3.0%
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  • Purpose

    Sunscreen

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  • Uses

    • minimal sun protection product
    • minimal protection against sunburn and tanning
    • for skin that burns minimally
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  • Warnings

    For external use only

    When using this product

    • keep out of eyes. Rinse with water to remove

    Stop use and ask a doctor if

    • rash or irritation develops and lasts.

    Keep Out of the reach of children.

    If swallowed get medical help or contact a Poison Control Center right away.

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  • Directions

    • do not spray directly on face
    • apply generously and evenly before sun exposure and as needed
    • reapply frequently and after towel drying, swimming or perspiring.
    • this product is not recommended for use on children
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  • Inactive ingredients

    Mineral Oil, Isopropyl Myristate, Sesamum Indicum (Sesame) Seed Oil, Persea Gratissima (Avocado) Oil, Amyl Acetate, Cocos Nucifera (Coconut) Oil, Squalane, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract, Aleurites Moluccana Seed Extract, Carica Papaya (Papaya) Fruit Extract, Colocasia Antiquorum Root Extract, Mangifera Indica (Mango) Fruit Extract, Passiflora Incarnata Fruit Extract, Plumeria Acutifolia Flower Extract, Psidium Guajava Fruit Extract, Eucalyptus Globulus Leaf Oil, Fragrance.
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  • Principal Display Panel

    Walgreens
    NEW
    DARK
    TANNING OIL
    SUNSCREEN
    SPF
    4
    8 FL. OZ. (237 mL)
    ZWA017A0.jpg
    ZWA017A0b.jpg
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  • INGREDIENTS AND APPEARANCE
    WALGREENS DARK TANNING OIL SUNSCREEN  SPF 4
    octinoxate spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-4004
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    MINERAL OIL (UNII: T5L8T28FGP)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    AMYL ACETATE (UNII: 92Q24NH7AS)  
    PAPAYA (UNII: KU94FIY6JB)  
    COLOCASIA ESCULENTA ROOT (UNII: H7B71Q0G0D)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P)  
    GUAVA (UNII: 74O70D6VG0)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    MANGO (UNII: I629I3NR86)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    PLUMERIA RUBRA FLOWER (UNII: 8P7XXY759H)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-4004-16 226 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 12/04/2012
    Labeler - WALGREEN CO. (008965063)
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