Label: WALGREENS DAYTIME FACIAL MOISTURIZER WITH BROAD SPECTRUM SPF 30 SUNSCREEN- homosalate, octocrylene, zinc oxide lotion
- NDC Code(s): 0363-0187-03
- 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 20, 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, Niacinamide, Glycerin, Cetearyl Alcohol, Dimethicone, Cetearyl Glucoside, Ceramide NP, Ceramide AP, Ceramide EOP, Sodium Hyaluronate, Aluminum Starch Octenylsuccinate, Boron Nitride, Hydroxyethylcellulose, Disodium EDTA, Cetyl Palmitate, Sorbitan Palmitate, Sorbitan Olivate, Phenoxyethanol, Capryloyl Glycine, Undecylenoyl Glycine, Triethoxycaprylylsilane, Sodium Lauroyl Lactylate, Phytosphingosine, Cholesterol, Carbomer, Xanthan Gum.
- Label
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INGREDIENTS AND APPEARANCE
WALGREENS DAYTIME FACIAL MOISTURIZER WITH BROAD SPECTRUM SPF 30 SUNSCREEN
homosalate, octocrylene, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0187 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 63 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength CERAMIDE NP (UNII: 4370DF050B) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) CERAMIDE AP (UNII: F1X8L2B00J) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) CETYL PALMITATE (UNII: 5ZA2S6B08X) BORON NITRIDE (UNII: 2U4T60A6YD) CHOLESTEROL (UNII: 97C5T2UQ7J) HEXAMETHYLDISILOXANE (UNII: D7M4659BPU) HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SORBITAN MONOPALMITATE (UNII: 77K6Z421KU) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) UNDECYLENOYL GLYCINE (UNII: 4D20464K2J) NIACINAMIDE (UNII: 25X51I8RD4) SORBITAN OLIVATE (UNII: MDL271E3GR) XANTHAN GUM (UNII: TTV12P4NEE) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) EDETATE DISODIUM (UNII: 7FLD91C86K) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0187-03 1 in 1 CARTON 06/26/2019 1 89 mL in 1 BOTTLE; 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 06/26/2019 Labeler - WALGREEN COMPANY (008965063)
