Label: WALGREENS ADVANCED 50 HYDRATING BROAD SPECTRUM SPF 50 SUNSCREEN- avobenzone. homosalate, octisalate, octocrylene lotion
- NDC Code(s): 0363-0233-15
- Packager: WALGREEN COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 April 24, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
- apply liberally 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
- children under 6 months of age: Ask a doctor
- 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, BUTYLOCTYL SALICYLATE, NEOPENTYL GLYCOL DIHEPTANOATE, GLYCERYL STEARATE, GLYCERIN, CETEARYL OLIVATE, PEG-100 STEARATE, SORBITAN OLIVATE, STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER, VP/HEXADECENE COPOLYMER, C30-38 OLEFIN/ISOPROPYL MALEATE/MA COPOLYMER, ETHYLHEXYLGLYCERIN, XANTHAN GUM, POLYMETHYL METHACRYLATE, CHLORPHENESIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL, CARNOSINE, FRAGRANCE, CERAMIDE NP, SODIUM HYALURONATE, BUTYLENE GLYCOL, ALTEROMONAS FERMENT EXTRACT, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, TETRASODIUM EDTA, CITRIC ACID, SODIUM HYDROXIDE.
- Label
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INGREDIENTS AND APPEARANCE
WALGREENS ADVANCED 50 HYDRATING BROAD SPECTRUM SPF 50 SUNSCREEN
avobenzone. homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0233 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 40 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 90 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CARNOSINE (UNII: 8HO6PVN24W) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SOYBEAN (UNII: L7HT8F1ZOD) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL 1-STEARATE (UNII: 258491E1RZ) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETEARYL OLIVATE (UNII: 58B69Q84JO) CHLORPHENESIN (UNII: I670DAL4SZ) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) SORBITAN OLIVATE (UNII: MDL271E3GR) VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9) CERAMIDE NP (UNII: 4370DF050B) ALTEROMONAS MACLEODII POLYSACCHARIDES (UNII: AP6XG2GR8Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) STEARYL/OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: PN88NW0KPK) EDETATE SODIUM (UNII: MP1J8420LU) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0233-15 1 in 1 CARTON 10/16/2019 1 148 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 final M020 10/16/2019 Labeler - WALGREEN COMPANY (008965063)