![OH MY BOD SPF50 ANTIOXIDANT INFUSED DRY TOUCH SUNSCREEN (BUTYL METHOXYDIBENZOYLMETHANE, HOMOSALATE, OCTOCRYLENE, OCTYL SALICYLATE) CREAM [EVERYDAY GROUP LIMTED]](https://medic.hrt.org//dailymed/images/48e70326-ecf7-44c9-a4cc-2044bd6a6415/Updated Design OMB.jpg)
| NDC | 72098-002-03 |
| Set ID | 48e70326-ecf7-44c9-a4cc-2044bd6a6415 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Everyday Group Limted |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART352 |
- 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
- 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
- Other information
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Inactive ingredients
Water (Aqua), Cera Alba, C12-15 Alkyl Benzoate, PEG-15 Cocamine, Silica, Caprylyl Glycol, PEG-40 Stearate, Hydroxyethylcellulose, Carbomer, Triethanolamine, Aloe Barbadnesis Leaf Juice, Tocopheryl Acetate, Simmondsia Chinensis Seed Oil, Glycerin, Carthamus Tinctorius Seed Oil, Cucumis Sativus Fruit Extract, Camellia Sinensis Leaf Extract, Caprylhydroxamic Acid
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
OH MY BOD SPF50 ANTIOXIDANT INFUSED DRY TOUCH SUNSCREEN
butyl methoxydibenzoylmethane, homosalate, octocrylene, octyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72098-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL 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 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) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-40 STEARATE (UNII: ECU18C66Q7) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) JOJOBA OIL (UNII: 724GKU717M) GLYCERIN (UNII: PDC6A3C0OX) SAFFLOWER OIL (UNII: 65UEH262IS) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72098-002-03 1 in 1 BOX 03/09/2020 1 100 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 not final part352 03/09/2020 Labeler - Everyday Group Limted (664624682)
