Label: HEB SPF 50 SHINE SUNSCREEN WITH VITAMIN C CONTINUOUS SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 37808-193-37
- Packager: H.E.B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 26, 2025
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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
- 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
-
Inactive Ingredients
acrylates/octylacrylamide copolymer, aloe barbadensis leaf juice, ascorbic acid, butylene glycol, butyloctyl salicylate, camellia sinensis leaf extract, caprylic/capric triglyceride, citrus aurantifolia (lime) oil, citrus aurantium dulcis (orange) peel oil, citrus grandis (grapefruit) peel oil, citrus limon (lemon) peel oil, fragrance, glycerin, helianthus annuus (sunflower) seed oil, olea europaea (olive) fruit oil, panthenol, propylene glycol, saccharomyces/ podophyllum peltatum ferment filtrate, SD alcohol 40-B, tocopherol, water
- Label
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INGREDIENTS AND APPEARANCE
HEB SPF 50 SHINE SUNSCREEN WITH VITAMIN C CONTINUOUS SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-193 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 CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0) GRAPEFRUIT OIL (UNII: YR377U58W9) LEMON OIL (UNII: I9GRO824LL) LIME OIL (UNII: UZH29XGA8G) PANTHENOL (UNII: WV9CM0O67Z) OLIVE OIL (UNII: 6UYK2W1W1E) WATER (UNII: 059QF0KO0R) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ASCORBIC ACID (UNII: PQ6CK8PD0R) SUNFLOWER OIL (UNII: 3W1JG795YI) 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) PODOPHYLLUM (UNII: 2S713A4VP3) ORANGE OIL (UNII: AKN3KSD11B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-193-37 156 g in 1 CAN; Type 0: Not a Combination Product 01/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/03/2024 Labeler - H.E.B (007924756)
