Label: SPF 55 SPORT SUNSTICK WELL AT WALGREENS- avobenzone - 3.0% homosalate - 15.0% octisalate - 5.0% octocrylene - 10.0% oxybenzone - 6.0% stick
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-3215-01 - Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 13, 2018
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- Official Label (Printer Friendly)
- Active ingredients Purpose
- INDICATIONS & USAGE
- PURPOSE
- 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 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 sleeve shirts, pants, hats, and sunglasses
• Children under 6 month: Ask a doctor - Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SPF 55 SPORT SUNSTICK WELL AT WALGREENS
avobenzone - 3.0% homosalate - 15.0% octisalate - 5.0% octocrylene - 10.0% oxybenzone - 6.0% stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-3215 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) Avobenzone 3 g in 100 g Homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) Homosalate 15 g in 100 g Octocrylene (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) Octocrylene 10 g in 100 g Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) Octisalate 5 g in 100 g Oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) Oxybenzone 6 g in 100 g Inactive Ingredients Ingredient Name Strength CETEARYL BEHENATE (UNII: 7ARI9LTH0U) YELLOW WAX (UNII: 2ZA36H0S2V) Cetyl Alcohol (UNII: 936JST6JCN) Lauryl Laurate (UNII: GPW77G0937) Myristyl Myristate (UNII: 4042ZC00DY) Phenoxyethanol (UNII: HIE492ZZ3T) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ) COCOA BUTTER (UNII: 512OYT1CRR) Tocopherol (UNII: R0ZB2556P8) BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-3215-01 14 g in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/15/2014 Labeler - Walgreens (008965063) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(0363-3215) , label(0363-3215)