Label: BEET THE SUN LIGHTWEIGHT SUNSCREEN BROAD SPECTRUM SPF 40 PA- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 83493-150-01
- Packager: Krave Beauty, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating
- Reapply at least every 2 hours
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures.
- limit time in the sun, especially from 10 a.m.-2 p.m. / Wear long sleeved shirts, pants, hats and sunglasses
- Children under 6 months: Ask a doctor
- Other information
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Inactive Ingredients
Water (Aqua), Propanediol, Pentylene Glycol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Bisabolol, Ethylhexyl Methoxycrylene, Hydroxyacetophenone, Beta Vulgaris (Beet) Root Extract, Isohexadecane, Polysorbate 80, Hyaluronic Acid, Tocopheryl Acetate, Caprylyl Glycol, Eugenia Caryophyllus Bud Extract, Solidago Virgaurea Extract, Salix Alba (Willow) Bark Extract, Trisodium Ethylenediamine Disuccinate, 1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Citric Acid, Sodium Hydroxide
- Package Labeling:
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INGREDIENTS AND APPEARANCE
BEET THE SUN LIGHTWEIGHT SUNSCREEN BROAD SPECTRUM SPF 40 PA
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83493-150 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 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) PENTYLENE GLYCOL (UNII: 50C1307PZG) LEVOMENOL (UNII: 24WE03BX2T) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) BEET (UNII: N487KM8COK) ISOHEXADECANE (UNII: 918X1OUF1E) POLYSORBATE 80 (UNII: 6OZP39ZG8H) HYALURONIC ACID (UNII: S270N0TRQY) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SALIX ALBA BARK (UNII: 205MXS71H7) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) XANTHAN GUM (UNII: TTV12P4NEE) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83493-150-01 50 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/01/2023 Labeler - Krave Beauty, LLC (086662891)
