Label: BATH AND BODY WORKS SPF AT THE BEACH- avobenzone,homosalate,octisalate,octocrylene lotion
- NDC Code(s): 62670-6685-0, 62670-6685-1
- Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 28, 2024
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- 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 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 • children under 6 months: Ask a doctor
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Inactive ingredients
Water (Aqua, Eau), Butyloctyl Salicylate, Glycerin, Styrene/Acrylates Copolymer, Glyceryl Stearate, PEG-100 Stearate, Butylene Glycol, VP/Hexadecene Copolymer, Fragrance (Parfum), Phenoxyethanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxyacetophenone, Diethylhexyl 2,6-Naphthalate, PEG-8 Laurate, Chlorphenesin, Xanthan Gum, Oryza Sativa (Rice) Bran Extract, Tocopheryl Acetate, Sodium Hydroxide, Tetrasodium Glutamate Diacetate, Ethylhexylglycerin, Helianthus Annuus (Sunflower) Extract, Tocopherol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Limonene, Hydroxycitronellal, Coumarin, Benzyl Salicylate, Hexyl Cinnamal, Linalool
- Other information
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INGREDIENTS AND APPEARANCE
BATH AND BODY WORKS SPF AT THE BEACH
avobenzone,homosalate,octisalate,octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6685 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 mg in 100 mg AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 mg in 100 mg HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 mg in 100 mg OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 mg in 100 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62670-6685-0 74 mg in 1 BOTTLE; Type 0: Not a Combination Product 02/12/2024 2 NDC:62670-6685-1 117 mg in 1 BOTTLE; Type 0: Not a Combination Product 02/12/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2024 Labeler - Bath & Body Works, Inc. (878952845) Establishment Name Address ID/FEI Business Operations KDC/ONE Chatsworth, Inc. 118542196 manufacture(62670-6685)