Label: OH MY BOD SPF 50 SUNSCREEN- homosalate, octocrylene, octisalate, avobenzone lotion
- NDC Code(s): 72098-005-05, 72098-005-06
- Packager: EVERYDAY GROUP LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- 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
- Spending time in the sun increases your risk of skin cancer and ealy skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures:
- Limit time in the sun, especially from 10 a.m. to 2 p.m.
- Wear long-sleeved shirts, pants, hats, and suglasses
- Children under 6 months of age: Ask a doctor
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Inactive Ingredients
Water (Aqua), Cera Alba, C12-15 Alkyl Benzoate, PEG-15 Cocamine, Silica, Sodium Hyaluronate, Alteromonas Ferment Extract, Simmondsia Chinensis Seed Oil, Carthamus Tinctorius Seed Oil, Cucumis Sativus Fruit Extract, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Caprylyl Glycol, PEG-40 Stearate, Butylene Glycol, Hydroxyethylcellulose, Carbomer, Caprylhydroxamic Acid, Glycerin, Triethanolamine, Potassium Sorbate, Parfum* *Natural Fragrance
- Other Information
- Package Labeling:72098-003-05
- Package Labeling:72098-003-06
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INGREDIENTS AND APPEARANCE
OH MY BOD SPF 50 SUNSCREEN
homosalate, octocrylene, octisalate, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72098-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) WHITE WAX (UNII: 7G1J5DA97F) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) PEG-15 COCAMINE (UNII: 8L6LB12TSJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z) JOJOBA OIL (UNII: 724GKU717M) SAFFLOWER OIL (UNII: 65UEH262IS) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-40 STEARATE (UNII: ECU18C66Q7) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72098-005-05 100 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2021 2 NDC:72098-005-06 1 in 1 BOX 12/01/2021 2 30 mL 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 12/01/2021 Labeler - EVERYDAY GROUP LIMITED (664624682)
