Label: 6000X ELEMENTAL SCREEN BS SPF 30 SUNSCREEN- zinc oxide cream
- NDC Code(s): 62742-4241-1, 62742-4241-2
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions • Apply liberally 15 minutes before sun exposure • Use a water-resistant sunscreen if swimming or sweating • Children under 6 months: Ask a doctor • Reapply: • after swimming or sweating • immediately after towel drying • at least every 2 hours • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10am - 2pm • wear long-sleeve shirts, pants, hats, and sunglasses.
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive Ingredients:
Caprylic/Capric Triglyceride, Water (Aqua), Glycerin, Polysorbate 60*, Sorbitan Stearate, Stearic Acid, Cetearyl Glucoside, Cetyl Alcohol, Astaxanthin, Niacinamide (Vitamin B3), Ferulic Acid, Tocopherol (Vitamin E), Totarol (Podocarpus Totara), Mel (Manuka Honey), Phormium Tenax (Harakeke) Seed Oil, Gardenia Jasminoides Meristem Cell Culture, Punica Granatum (Pomegranate) Extract, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Aloe Barbadensis Leaf Juice, Carrageenan, Lecithin, Xanthan Gum, Sodium Phytate, Isostearic Acid, Polyhydroxystearic Acid, Polyglyceryl-3 Polyricinoleate, Dehydroacetic Acid, Stearyl Alcohol, Benzyl Alcohol. *Tween 60-LQ(AP)
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
6000X ELEMENTAL SCREEN BS SPF 30 SUNSCREEN
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4241 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 18.9 g in 100 g Inactive Ingredients Ingredient Name Strength SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549) ALMOND OIL (UNII: 66YXD4DKO9) ALOE VERA LEAF (UNII: ZY81Z83H0X) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PHYTATE SODIUM (UNII: 88496G1ERL) ISOSTEARIC ACID (UNII: X33R8U0062) CETYL ALCOHOL (UNII: 936JST6JCN) NIACINAMIDE (UNII: 25X51I8RD4) TOTAROL (UNII: 67NH2854WW) PHORMIUM TENAX SEED OIL (UNII: OZ80CEA779) CARRAGEENAN (UNII: 5C69YCD2YJ) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) GLYCERIN (UNII: PDC6A3C0OX) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) FERULIC ACID (UNII: AVM951ZWST) TOCOPHEROL (UNII: R0ZB2556P8) HONEY (UNII: Y9H1V576FH) STEARIC ACID (UNII: 4ELV7Z65AP) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ASTAXANTHIN (UNII: 8XPW32PR7I) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) XANTHAN GUM (UNII: TTV12P4NEE) POLYSORBATE 60 (UNII: CAL22UVI4M) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) DEHYDROACETIC ACID (UNII: 2KAG279R6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4241-2 1 in 1 CARTON 12/12/2023 1 NDC:62742-4241-1 59 g 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 12/12/2023 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4241)