Label: HEB SPF 50 REFINE 50 SUNSCREEN WITH NIACINAMIDE AND COLLAGEN CONTINUOUS SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 37808-142-37
- Packager: H.E.B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 15, 2024
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- 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
- apply liberally 15 minutes before sun exposure
- hold can 4-6 inches away from body, spray evenly to ensure complete coverage
- do not spray into face. Spray into hand and apply to face.
- use in well ventilated, but not windy areas
- 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.
• wearl long-sleeved shirts, pants, hats, and sunglasses
- Other Information
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Inactive Ingredients
SD ALCOHOL 40-B, BUTYLOCTYL SALICYLATE, FRAGRANCE, ACRYLATES/OCTYLACRYLAMIDE COPOLYMER, ALOE BARBADENSIS LEAF JUICE, BUTYLENE GLYCOL, SACCHAROMYCES/ PODOPHYLLUM PELTATUM FERMENT FILTRATE, DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT, PANTHENOL, PERSEA GRATISSIMA (AVOCADO) OIL, VITIS VINIFERA (GRAPE) SEED OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, COCOS NUCIFERA (COCONUT) OIL, CAPRYLIC/CAPRIC TRIGLYCERIDE, GLYCERIN, STEAROXYTRIMETHYLSILANE, TOCOPHEROL, HYDROLYZED COLLAGEN, NIACINAMIDE.
- Label
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INGREDIENTS AND APPEARANCE
HEB SPF 50 REFINE 50 SUNSCREEN WITH NIACINAMIDE AND COLLAGEN CONTINUOUS SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-142 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 BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C) PODOPHYLLUM (UNII: 2S713A4VP3) WATER (UNII: 059QF0KO0R) CARROT (UNII: L56Z1JK48B) ALOE VERA LEAF (UNII: ZY81Z83H0X) PANTHENOL (UNII: WV9CM0O67Z) JOJOBA OIL (UNII: 724GKU717M) ALCOHOL (UNII: 3K9958V90M) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) GRAPE SEED OIL (UNII: 930MLC8XGG) COCONUT OIL (UNII: Q9L0O73W7L) AVOCADO OIL (UNII: 6VNO72PFC1) STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2) NIACINAMIDE (UNII: 25X51I8RD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-142-37 156 g in 1 CAN; Type 0: Not a Combination Product 01/27/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/27/2022 Labeler - H.E.B (007924756)
