Label: EQUATE SUNSCREEN FOR ALL SKIN TONES SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 79903-251-12
- Packager: WAL-MART INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 2, 2024
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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
• 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
aluminum starch octenylsuccinate, aminomethyl propanol, benzyl alcohol, butyrospermum parkii (shea) butter, caprylyl glycol, carbomer, dimethicone, disodium EDTA, ethylhexylglycerin, fragrance, persea gratissima (avocado) oil, phenoxyethanol, polyethyloxazoline, polyglyceryl-3 distearate, simmondsia chinensis (jojoba) seed oil, sorbitan isostearate, sorbitol, stearic acid, tocopherol, tridecyl salicylate, water
- Label
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INGREDIENTS AND APPEARANCE
EQUATE SUNSCREEN FOR ALL SKIN TONES SPF 50
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-251 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 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 150 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70 mg in 1 mL Inactive Ingredients Ingredient Name Strength SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BENZYL ALCOHOL (UNII: LKG8494WBH) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HEXAMETHYLDISILOXANE (UNII: D7M4659BPU) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) SORBITOL (UNII: 506T60A25R) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8) TOCOPHEROL (UNII: R0ZB2556P8) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) AVOCADO OIL (UNII: 6VNO72PFC1) JOJOBA OIL (UNII: 724GKU717M) SHEA BUTTER (UNII: K49155WL9Y) POLYETHYLOXAZOLINE (200000 MW) (UNII: I765I75FT2) POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-251-12 237 mL in 1 TUBE; Type 0: Not a Combination Product 02/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/01/2024 Labeler - WAL-MART INC. (051957769)
