Label: ULTRA VIOLETTE VIBRANT SCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 84803-102-00
- Packager: Grace and Fire USA Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 10, 2024
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- ACTIVE INGREDIENTS
- SUNSCREEN
- USE
- WARNINGS
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Directions
Directions for Sunscreen Use
apply liberally and evenly 15 minutes before sun exposure
reapply at least every 2 hours
use a water resistant sunscreen if swimming or sweating
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
children under 6 months of age: Ask a doctor
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Inactive Ingredients
Water, Cera Alba, Cyclopentasiloxane, Cetearyl Alcohol, Isopropyl Palmitate, Ceteareth-20, Cyclohexasiloxane, Benzyl Alcohol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Hydroxyacetophenone, Saccharide Isomerate, Mica, Phenoxyethanol, Triethanolamine, Sodium Stearoyl Glutamate, Carbomer, Fragrance, Citric Acid, Sodium Citrate, Benzyl Salicylate, Hexyl Cinnamal, Linalool, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491).
- Other information
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INGREDIENTS AND APPEARANCE
ULTRA VIOLETTE VIBRANT SCREEN BROAD SPECTRUM SPF 50
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84803-102 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 OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) BENZYL SALICYLATE (UNII: WAO5MNK9TU) LINALOOL, (+/-)- (UNII: D81QY6I88E) CETEARETH-20 (UNII: YRC528SWUY) WATER (UNII: 059QF0KO0R) CYCLOPENTASILOXANE (UNII: 0THT5PCI0R) BENZYL ALCOHOL (UNII: LKG8494WBH) ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X) SACCHARIDE ISOMERATE (UNII: W8K377W98I) MICA (UNII: V8A1AW0880) TRIETHANOLAMINE (UNII: 9O3K93S3TK) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) CARBOMER (UNII: 0A5MM307FC) CI 77891 (UNII: 15FIX9V2JP) WHITE WAX (UNII: 7G1J5DA97F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID (UNII: 2968PHW8QP) SODIUM CITRATE (UNII: 1Q73Q2JULR) CETEARYL ALCOHOL (UNII: 2DMT128M1S) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CI 77491 (UNII: 1K09F3G675) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) HEXYL CINNAMAL (UNII: 7X6O37OK2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84803-102-00 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/01/2024 Labeler - Grace and Fire USA Inc. (119357605)
