Label: BEACH GYPSY GLITTER SUNSCREEN SPF 30- octinoxate, octocrylene, octisalate, avobenzone cream
- NDC Code(s): 72085-312-05
- Packager: MJ Products Association, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 5, 2023
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- Drug Facts
- ACTIVE INGREDIENTS
- USES
- WARNINGS
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Directions
- Apply liberally 15 minutes before sun exposure.
- At least every two-hours.
- Immediately after swimming, sweating or towel drying. SUN PROTECTION MEASURES: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use suncreen with broad spectrum protection and on SPF rating of 15 or higher, along with other sun protection measures including: Limit time in the sun, especially between 10am and 2pm.
- Wear long sleeve shirts, pants, hats, and sunglasses.
- For children under 6 months, consult a physician.
REAPPLY:
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Other Ingredients
Aloe Barbadensis Leaf (Aloe Vera Gel), Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Camellia Sinensis (Green Tea) Extract, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Cocos Nucifera (Coconut) Oil, Daucus Carota Sativa (Carrot) Seed Oil, Ethylhexylglycerin, Glitter: Regenerated Cellulose/Rayon, FD&C Yellow #5, Aluminum; Glyceryl Stearate, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Sorbitan Olivate, Tocopherol Acetate (Vitamin E), Zemea (Corn) Propanediol.
- Other Information
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INGREDIENTS AND APPEARANCE
BEACH GYPSY GLITTER SUNSCREEN SPF 30
octinoxate, octocrylene, octisalate, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72085-312 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 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGAN OIL (UNII: 4V59G5UW9X) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCONUT OIL (UNII: Q9L0O73W7L) CARROT SEED OIL (UNII: 595AO13F11) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) REGENERATED CELLULOSE (UNII: BX81F82EWG) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) ALUMINUM (UNII: CPD4NFA903) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) SORBITAN OLIVATE (UNII: MDL271E3GR) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CORN (UNII: 0N8672707O) PROPANEDIOL (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72085-312-05 5 mL in 1 PACKET; Type 0: Not a Combination Product 08/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/10/2020 Labeler - MJ Products Association, LLC (081022202)