Label: EQUATE SUNSCREEN KIDS SPF50 BROAD SPECTRUM- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 49035-845-37, 49035-845-48, 49035-845-63, 49035-845-78
- Packager: WAL-MART STORES INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- 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
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Inactive ingredients
alcohol denat., isododecane, diisopropyl adipate, acrylates/octylacrylamide copolymer, VA/butyl maleate/isobornyl acrylate copolymer, PEG-12 dimethicone, caprylyl glycol, hydrogenated methyl abietate, ascorbyl palmitate, tocopheryl acetate, mineral oil, panthenol, water, aloe barbadensis leaf extract, fragrance
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EQUATE SUNSCREEN KIDS SPF50 BROAD SPECTRUM
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-845 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MINERAL OIL (UNII: T5L8T28FGP) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) DIISOPROPYL ADIPATE (UNII: P7E6YFV72X) ASCORBYL PALMITATE (UNII: QN83US2B0N) PANTHENOL (UNII: WV9CM0O67Z) ISODODECANE (UNII: A8289P68Y2) METHYL HYDROGENATED ROSINATE (UNII: 13DHA19W9N) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-845-37 156 g in 1 CAN; Type 0: Not a Combination Product 01/04/2017 2 NDC:49035-845-63 2 in 1 PACKAGE 01/04/2017 2 NDC:49035-845-37 156 g in 1 CAN; Type 0: Not a Combination Product 3 NDC:49035-845-48 258 g in 1 CAN; Type 0: Not a Combination Product 01/04/2017 4 NDC:49035-845-78 516 g in 1 CAN; Type 0: Not a Combination Product 01/04/2017 01/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/04/2017 Labeler - WAL-MART STORES INC (051957769)