KROGER SUNSCREEN SPF 8 (OCTINOXATE OXYBENZONE) LOTION [THE KROGER CO]

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  • KROGER SUNSCREEN SPF 8 (OCTINOXATE OXYBENZONE) LOTION [THE KROGER CO]

KROGER SUNSCREEN SPF 8 (OCTINOXATE OXYBENZONE) LOTION [THE KROGER CO]
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NDC 30142-925-56
Set ID 8bd6cda7-fac8-46ae-9519-ef4725e13cea
Category HUMAN OTC DRUG LABEL
Packager THE KROGER CO
Generic Name
Product Class
Product Number
Application Number PART352
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  • Active ingredients

    Octinoxate 7.5%
    Oxybenzone 2.0%
  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • higher SPF gives more sunburn protection
    • retains SPF after 80 minutes of activity in the water
  • 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 reach of children.

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

  • Directions


    • apply generously and evenly before sun exposure and as needed
    • children under 6 months of age:ask a doctor
    • reapply frequently and after towel drying, swimming or perspiring.
  • Other Information

    • May stain some fabrics
    • Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.
  • Inactive Ingredients

    Water, Ethylhexyl Palmitate, Propylene Glycol, Cetyl Phosphate, Triethanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Powder, Diazolidinyl Urea, Methylparaben, Propylparaben, Fragrance.

    For comments or questions
    please call 1-800-632-6900
  • Principal Display Panel

    kroger
    QUALITY GUARANTEED
    Sunscreen 8 spf
    SUNSCREEN LOTION
    with
    Aloe and Vitamin E
    Very
    Water
    Resistant
    8 FL OZ (236 mL)
    ZKR009A0.jpg
  • INGREDIENTS AND APPEARANCE
    KROGER SUNSCREEN  SPF 8
    octinoxate oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-925
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 g  in 100 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CETYL PHOSPHATE (UNII: VT07D6X67O)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-925-56226 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35211/12/2012
    Labeler - THE KROGER CO (006999528)
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