Label: WALGREENS 40 INVISIBLE FACIAL SUNSCREEN BROAD SPECTRUM SPF 40- avobenzone, homosalate, octisalate, octocrylene gel
- NDC Code(s): 0363-0349-17
- Packager: WALGREEN COMPANY
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 11, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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.
-
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
- 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
-
Inactive ingredients
dimethicone/bis-isobutyl PPG-20 crosspolymer, isododecane, caprylic/capric triglyceride, microcrystalline cellulose, isohexadecane, tocopherol, dicaprylyl carbonate, lithothamnion calcareum powder, meadowfoam estolide, olibanum, jojoba esters, lecithin, neopentyl glycol diheptanoate, polyester-7, silica, polymethylsilsesquioxane, mannitol, diatomaceous earth, zinc sulfate
- Label
-
INGREDIENTS AND APPEARANCE
WALGREENS 40 INVISIBLE FACIAL SUNSCREEN BROAD SPECTRUM SPF 40
avobenzone, homosalate, octisalate, octocrylene gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0349 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF) ISOHEXADECANE (UNII: 918X1OUF1E) ISODODECANE (UNII: A8289P68Y2) POLYESTER-7 (UNII: 0841698D2F) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) MANNITOL (UNII: 3OWL53L36A) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K) DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK) MEADOWFOAM ESTOLIDE (UNII: 3HH93SL2H9) ZINC SULFATE ANHYDROUS (UNII: 0J6Z13X3WO) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0349-17 50 mL in 1 TUBE; Type 0: Not a Combination Product 10/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/19/2023 Labeler - WALGREEN COMPANY (008965063)
