Label: SEA STAR SPARKLE SPF-50 VERY BERRY- octinoxate, octisalate, octocrylene, zinc oxide cream
- NDC Code(s): 72085-149-04
- Packager: MJ Products Association, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 11, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
-
Directions
- Apply liberally 15 minutes before sun exposure. REAPPLY:
- At least every two-hours.
- Immediately after swimming, sweating or towel drying. : Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: SUN PROTECTION MEASURES
- Limit time in the sun, especially between 10am to 2pm.
- Wear long sleeve shirts, pants, hats and sunglasses.
- For children under 6 months, consult a physician.
-
Other Ingredients
Acrylates Copolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Ethylhexylglycerin, : Polyethylene Terephthalate, Polymethyl Methacrylate, Polyurethane-33, FD&C Yellow #5, D&C Red #7, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Sorbitan Olivate, Styrene/Acrylates Copolymer, Tocopherol Acetate (Vitamin E), Zemea (Corn) Propanediol. Glitter
- Other information
- Questions or comments?
- Package Labeling
-
INGREDIENTS AND APPEARANCE
SEA STAR SPARKLE SPF-50 VERY BERRY
octinoxate, octisalate, octocrylene, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72085-149 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 50 mg in 1 g Inactive Ingredients Ingredient Name Strength BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 7 (UNII: ECW0LZ41X8) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITAN OLIVATE (UNII: MDL271E3GR) STYRENE (UNII: 44LJ2U959V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72085-149-04 113 g in 1 TUBE; Type 0: Not a Combination Product 03/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/01/2018 Labeler - MJ Products Association, LLC (081022202)