Label: DEFEND TATTOO SUNSCREEN SPF 30- zinc oxide cream
- NDC Code(s): 80396-079-00
- Packager: Rabbit Mad Tattoo LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 6, 2023
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- Drug Facts
- Active Ingredient
- Uses:
- Warnings:
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Directions:
• Apply liberally 15 minutes before sun exposure and as needed. • Children under 6 months of age: ask a doctor. • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating • Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF 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.
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Inactive Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbic Acid (Vitamin C), Benzyl Alcohol, Butyloctyl Salicylate, Calendula Officinalis Extract, Caprylic/Capric Triglyceride, Chamomilla Recutita (Chamomile) Extract, Cucumis Sativus(Cucumber) Extract, Daucus Carota Sativa (Carrot) Extract, Decyl Glucoside, Dehydroacetic Acid, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Hydroxyethylcellulose, Polyhydroxystearic Acid, Rosa Canina (Rose) Hips Oil, Stearic Acid, Theobroma Cacao (Cocoa) Butter, Tocopheryl Acetate (Vitamin E), Xanthan Gum, Zemea (Corn) Propanediol.
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INGREDIENTS AND APPEARANCE
DEFEND TATTOO SUNSCREEN SPF 30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80396-079 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 140 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGAN OIL (UNII: 4V59G5UW9X) ASCORBIC ACID (UNII: PQ6CK8PD0R) BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CHAMOMILE (UNII: FGL3685T2X) CUCUMBER (UNII: YY7C30VXJT) CARROT (UNII: L56Z1JK48B) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ROSE OIL (UNII: WUB68Y35M7) STEARIC ACID (UNII: 4ELV7Z65AP) COCOA (UNII: D9108TZ9KG) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) XANTHAN GUM (UNII: TTV12P4NEE) CORN (UNII: 0N8672707O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80396-079-00 1 in 1 BOX 08/25/2020 1 100 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/25/2020 Labeler - Rabbit Mad Tattoo LLC (117625305)