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SCRUBS Solar Guard Sunscreen Wipe (ITW Dymon)

Available Formats

Dosage Form Package Information Links
CLOTH 9 mL in 1 PACKET (51239-0912-1) Label Information

Complete SCRUBS Solar Guard Sunscreen Wipe Information

  • ACTIVE INGREDIENT

    Active Ingredient                                                                                                          Purpose

    Homosalate (2%)..........................................................................................................Sunscreen

    Octinoxate (7.5%).........................................................................................................Sunscreen

    Octisalate (4%).............................................................................................................Sunscreen

    Oxybenzone (5%)........................................................................................................Sunscreen


  • PURPOSE

    Uses

    • Provides high protection against sunburn.
    • Retains SPF after 80 minutes of sweating or activity in the water.

  • WHEN USING

    Warnings

    For external use only.

    Flammable.  Keep away from heat and flame when applying this product.


  • 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 or irritation develops and lasts.

  • 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.


  • WHEN USING

    Directions

    • Unfold towel.
    • Apply evenly before sun exposure.
    • For children under 6 months, consult a doctor.
    • Reapply after towel drying, swimming or sweating.

  • QUESTIONS

    Inactive Ingredients

    Acrylates/Octylacrylamide Copolymer, Ethanol, Fragrance


  • INGREDIENTS AND APPEARANCE
    SCRUBS SOLAR GUARD SUNSCREEN WIPE  SCRUBS SOLAR GUARD
    sunscreen wipe cloth
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51239-0912
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HOMOSALATE (UNII: V06SV4M95S) (SALICYLIC ACID - UNII:O414PZ4LPZ) HOMOSALATE 20 g  in 856 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATE - UNII:93NOD9WBCS) OCTINOXATE 75 g  in 856 mL
    OCTISALATE (UNII: 4X49Y0596W) (SALICYLIC ACID - UNII:O414PZ4LPZ) OCTISALATE 40 g  in 856 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (BENZOPHENONE - UNII:701M4TTV9O) OXYBENZONE 50 g  in 856 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M) 80.1 g  in 856 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51239-0912-1 9 mL in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 03/01/2010
    Labeler - ITW Dymon (103307604)
    Registrant - ITW Dymon (103307604)
    Establishment
    Name Address ID/FEI Business Operations
    ITW Dymon 103307604 manufacture