Label: EQUATE SUNSCREEN SPF 50 SPORT BROADSPECTRUM- avobenzone,homosalate,octisalate,octocrylene spray
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NDC Code(s):
49035-843-37,
49035-843-39,
49035-843-48,
49035-843-63, view more49035-843-75, 49035-843-78
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- FLAMMABLE:
- 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
• Spray liberally and spread evenly by hand 15 minutes before sun exposure
• Hold can 4-6 inches away from the skin to apply
• Do not spray directly into face. Spray into hands then apply to face
• Do not apply in windy conditions
• Use in a well-ventilated area
• 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
- Label
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INGREDIENTS AND APPEARANCE
EQUATE SUNSCREEN SPF 50 SPORT BROADSPECTRUM
avobenzone,homosalate,octisalate,octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-843 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK) PANTHENOL (UNII: WV9CM0O67Z) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-843-48 258 g in 1 CAN; Type 0: Not a Combination Product 01/29/2019 2 NDC:49035-843-39 312 g in 1 CAN; Type 0: Not a Combination Product 01/29/2019 01/01/2020 3 NDC:49035-843-63 2 in 1 PACKAGE 01/29/2019 3 NDC:49035-843-37 156 g in 1 CAN; Type 0: Not a Combination Product 4 NDC:49035-843-75 624 g in 1 CAN; Type 0: Not a Combination Product 01/29/2019 12/02/2019 5 NDC:49035-843-78 516 g in 1 CAN; Type 0: Not a Combination Product 01/29/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/29/2019 Labeler - Walmart (051957769)