Label: BATH AND BODY WORKS SPF PINK PINEAPPLE SUNRISE- avobenzone,homosalate,octisalate,octocrylene lotion
- NDC Code(s): 62670-6686-0
- Packager: Bath & Body Works, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 1, 2024
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- 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, Hexyl Cinnamal.
- Other information
- SPL UNCLASSIFIED SECTION
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BATH AND BODY WORKS SPF PINK PINEAPPLE SUNRISE
avobenzone,homosalate,octisalate,octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62670-6686 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:62670-6686-0 117 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 02/12/2024 Labeler - Bath & Body Works, Inc. (878952845) Establishment Name Address ID/FEI Business Operations KDC/ONE Chatsworth, Inc. 118542196 manufacture(62670-6686)
