Label: LUCKY 13S ALL NATURAL TATTOO SUNSCREEN SPF-30- zinc oxide cream
- NDC Code(s): 82459-249-00
- Packager: SALES BRAIN HOLDINGS LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 11, 2023
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- DRUG FACTS
- ACTIVE INGREDIENTS:
- 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. • 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.
Sun Protection Measures. - OTHER INFORMATION:
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INACTIVE INGREDIENTS:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Benzyl Alcohol, Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Extract, Cannabis Sativus (Hemp) Seed Oil, Caprylic/Capric Triglyceride, Citric Acid, Citrullus Lanatus (Watermelon) Extract, Cocos Nucifera (Coconut) Oil, Decyl Glucoside, Dodecane, Dehydroacetic Acid, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Polyhydroxystearic Acid, Punica Granatum (Pomegranate) Extract, Stearic Acid, Tocopheryl Acetate (Vitamin E), Tridecyl Salicylate, Xanthan Gum, Zemea (Corn) Propanediol.
- Package Labeling:
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INGREDIENTS AND APPEARANCE
LUCKY 13S ALL NATURAL TATTOO SUNSCREEN SPF-30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82459-249 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) BENZYL ALCOHOL (UNII: LKG8494WBH) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) HEMP (UNII: TD1MUT01Q7) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATERMELON (UNII: 231473QB6R) COCONUT OIL (UNII: Q9L0O73W7L) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DODECANE (UNII: 11A386X1QH) DEHYDROACETIC ACID (UNII: 2KAG279R6R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) XANTHAN GUM (UNII: TTV12P4NEE) CORN (UNII: 0N8672707O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82459-249-00 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/13/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/13/2021 Labeler - SALES BRAIN HOLDINGS LLC (118327851)
