Label: SUN BUM 50 MINERAL SUNSCREEN 1 OZ- zinc oxide lotion
- NDC Code(s): 69039-797-01
- Packager: Sun Bum, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 13, 2025
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- Active Ingredients
- Purpose
- Uses
- Warnings
- Warnings
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Directions
• apply liberally 15 minutes before sun exposure
• reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
• children under 6 months of age: ask a doctor
• 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 value 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
- Directions
- Other Information
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Inactive Ingredients
METHYL DIHYDROABIETATE, TOCOPHEROL, POLYHYDROXYSTEARIC ACID, CITRIC ACID, BUTYROSPERMUM PARKII (SHEA) BUTTER, COCO-GLUCOSIDE, BUTYLOCTYL SALICYLATE, COCOS NUCIFERA (COCONUT) OIL, THEOBROMA CACAO (COCOA) SEED BUTTER, ETHYLHEXYLGLYCERIN, WATER, DIHEPTYL SUCCINATE, CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, SODIUM STEAROYL GLUTAMATE, CETEARYL ALCOHOL, ARACHIDYL ALCOHOL, CETYL ALCOHOL, BEHENYL ALCOHOL, BISABOLOL, ARACHIDYL GLUCOSIDE, MICROCRYSTALLINE CELLULOSE, CELLULOSE GUM, SODIUM HYALURONATE, SODIUM GLUCONATE, PHENOXYETHANOL
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- Primary Artwork
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INGREDIENTS AND APPEARANCE
SUN BUM 50 MINERAL SUNSCREEN 1 OZ
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69039-797 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CETEARYL ALCOHOL (UNII: 2DMT128M1S) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM GLUCONATE (UNII: R6Q3791S76) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) COCO-GLUCOSIDE (UNII: ICS790225B) THEOBROMA CACAO (COCOA) SEED BUTTER (UNII: 512OYT1CRR) BEHENYL ALCOHOL (UNII: 9G1OE216XY) CELLULOSE GUM (UNII: K679OBS311) SODIUM HYALURONATE (UNII: YSE9PPT4TH) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) CETYL ALCOHOL (UNII: 936JST6JCN) BISABOLOL (UNII: 24WE03BX2T) WATER (UNII: 059QF0KO0R) COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69039-797-01 30 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2025 Labeler - Sun Bum, LLC (028642574)
