Label: HEB SPF 50 REJUVENATE SUNSCREEN WITH MOISTURIZING OILS AND VITAMINS CONTINUOUS SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 37808-189-37
- Packager: H.E.B
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 27, 2025
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.
-
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, butylene glycol, butyloctyl salicylate, caprylic/capric triglyceride, cocos nucifera (coconut) oil, fragrance, glycerin, helianthus annuus (sunflower) seed oil, panthenol, persea gratissima (avocado) oil, saccharomyces/podophyllum peltatum ferment filtrate, SD alcohol 40-B, tocopherol
- Label
-
INGREDIENTS AND APPEARANCE
HEB SPF 50 REJUVENATE SUNSCREEN WITH MOISTURIZING OILS AND VITAMINS CONTINUOUS SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-189 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 COCONUT OIL (UNII: Q9L0O73W7L) AVOCADO OIL (UNII: 6VNO72PFC1) 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) PANTHENOL (UNII: WV9CM0O67Z) PODOPHYLLUM (UNII: 2S713A4VP3) SUNFLOWER OIL (UNII: 3W1JG795YI) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-189-37 156 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)
