Label: EPICUREN DISCOVERY SPF 30 - octinoxate and zinc oxide lotion 

  • Label RSS
  • NDC Code(s): 59663-130-04
  • Packager: Shine & Pretty (USA), Corp.
  • 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 07/13

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

  • Active Ingredients

    Octinoxate, 7.5% (UVB sunscreen), Zinc oxide, 10.0% (UVA/UVB sunscreen)

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  • Warnings

    For external use only, not to be swallowed. Avoid contact with eye. Discontinue if signs of irritation or rash appear.

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  • Purpose

    For Sun protection for surfaces of skin, face, arm and hand. SPF-15 provides the face and body skin with effective protection against harmful UVA and UVB rays. Use daily over moisture cream to help prevent premature aging and wrinkling due to prolonged exposure to the sun, reapply after swimming or excessive exercise.

    Paraben and PABA free.
    Fairly water resistant.
    Not tested on animals.

    Made in the USA specifically for professional dermatology and esthetic practices.

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  • Directions for Use

    Home Care: Apply SPF 30 liberally to face and body at least ten minutes before sun exposure or two minutes before applying makeup. Reapply after swimming or excessive perspiration. As part of effective age-fighting program, apply every morning throughout the year. Because SPF 30 is a blend of UV absorbing and reflecting sunscreens, it may be applied over or under moisturizer.

    Facial Procedure: SPF 30 is recommended as the finishing product at the end of the facial procedure for any skin type. It may be applied over finishing cream or moisturizer. It should not be rubbed in completely, but left on the skin until it becomes transparent.

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  • Inactive Ingredients

    Water, ethylhexyl palmitate, cyclomethicone, laurylmethicone, butylene glycol, tocopheryl acetate, sodium chloride, kukui (aleurites moluccana) seed oil (lipid-rich plant oil), green tea (camellia oleifera) seed extract, aloe vera (aloe barbadensis) leaf extract, tetrahexyldecyl ascorbate (time-released age-fighting vitamin C), allantoin, sodium PCA (hydrating), disodium EDTA, ethylhexylglycerin, methylisothiazolinone, fragrance (synthetic citrus).

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  • Questions?

    (805) 388-8581

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  • Keep out of the reach of children

    Keep Out of the reach of children. Use on children under six months of age only with the advice of a physician.

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  • Principal Panel Display

    MM1

    Label Graphic

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  • INGREDIENTS AND APPEARANCE
    EPICUREN DISCOVERY SPF 30 
    octinoxate, zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:59663-130
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (OCTINOXATE) OCTINOXATE 75 mg  in 1 mL
    ZINC OXIDE (ZINC OXIDE) ZINC OXIDE 100 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    VITAMIN A PALMITATE  
    CHAMOMILE  
    CUCUMBER  
    ETHYLHEXYL PALMITATE  
    CYCLOMETHICONE  
    BUTYLENE GLYCOL  
    .ALPHA.-TOCOPHEROL ACETATE  
    SODIUM CHLORIDE  
    KUKUI NUT  
    CAMELLIA OLEIFERA SEED  
    ALOE VERA LEAF  
    TETRAHEXYLDECYL ASCORBATE  
    ALLANTOIN  
    SODIUM PYRROLIDONE CARBOXYLATE  
    EDETATE DISODIUM  
    ETHYLHEXYLGLYCERIN  
    METHYLISOTHIAZOLINONE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59663-130-04 120 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 03/01/2013
    Labeler - Shine & Pretty (USA), Corp. (603528605)
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