Label: ARUBA ALOE VERY WATER RESISTANT SUNSCREEN SPF 50- octocrylene, octinoxate, oxybenzone, homosalate, octyl salicylate, avobenzone lotion
- NDC Code(s): 53675-158-08
- Packager: Aruba Aloe Balm NV
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- Uses
- Warnings
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Directions
- Apply generously before sun exposure and as needed
- Children under 6 months of age; ask a doctor
- Use sunscreens with broad spectrum SPF values of 15 or higher regularly and as directed
- Limit time in the sun, especially between the hours of 10 a.m. and 2 p.m., when the sun’s rays are most intense
- Wear clothing to cover skin exposed to the sun; for example, long-sleeved shirts, pants, sunglasses, and broad-brimmed hats
- Reapply sunscreen at least every 2 hours, more often if you’re sweating or jumping in and out of the water
- Inactive Ingredients
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DESCRIPTION
VERY WATER RESISTANT SUNSCREEN • BROAD SPECTRUM SPF 50+
Formulated with a unique blend of 100% Pure Aloe and Vitamin E, our Very Water Resistant Broad Spectrum SPF 50+ will leave your skin feeling soft and smooth while providing the sun protection your skin needs. Formulated to provide UVA/UVB Protection. For total sun care, apply our ultra-hydrating After Sun Lotion following prolonged exposure to the sun
Shop • Browse • Learn • www.ArubaAloe.com
Made in Aruba by Aruba Aloe Balm Inc. P.O. Box 360, Aruba Dutch Caribbean. Distributed in the USA by Aruba Aloe of North America LLC, Indianapolis, IN 46244. Customer Inquiry Hotline: 1-800-95-ARUBA.
This bottle contains 100% post-consumer recycled plastic. Please recycle. Aruba Aloe products are not tested 8.5 oz ( 251 mL) on animals.
- Product Labeling
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INGREDIENTS AND APPEARANCE
ARUBA ALOE VERY WATER RESISTANT SUNSCREEN SPF 50
octocrylene, octinoxate, oxybenzone, homosalate, octyl salicylate, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53675-158 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 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) ALOE VERA LEAF (UNII: ZY81Z83H0X) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) PENTAERYTHRITYL DISTEARATE (UNII: 697WOT8HNB) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLPARABEN (UNII: 14255EXE39) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53675-158-08 251 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/26/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/26/2013 Labeler - Aruba Aloe Balm NV (855442273)
