Label: ILLUMINIZING BLENDROPS BROAD SPECTRUM SPF 40- homosalate, octisalate, zinc oxide solution/ drops
- NDC Code(s): 44717-083-01
- Packager: Wasatch Product Development, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 26, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
Shake well and apply liberally 15 minutes prior to sun exposure. Reapply after swimming or perspiring, immediately after towel drying, at least every 2 hours.
Sun Protection Measures
Spending time in the sun increases your risk of skin cancer and early aging. To decrease the risk, regularyl use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.- 2p.m. Wear long sleeves shirts, pants, and sunglasses. Children under 6 months: ask a doctor.
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients
Water, Butyloctyl Salicylate, C12-15 Alkyl Benzoate. Titanium Dioxide (CI 77891), Mica, Propanediol, Coco-Caprylate/Caprate, Polyglyceryl-6 Stearate, Carthamus Tinctorius (Safflower) Oleosomes, Tranexamic Acid, PCA, Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Oryza Sativa (Rice) Bran Extract, Helianthus Annuus (Sunflower) Extract, Tocopherol, Gluconolactone, Polyglytamic Acid, Carthamus Tinctorius (Safflower) Seedcake Extract, Hydroxyethyl Acryleta/Sodium Acryloyldimethyl Taurate Copolymer, Polyhydroxystearic Acid, Cetyl Alcohol, Isopropryl Titanium Triisostearate, Iron Oxides (CI 77491), Synthetic Fluorphlogopite, Silica, Sodium Benzoate, 1,2-Hexanediol, Caprylyl Glycol, Caprylhydroxamic Acid, Hydroxyacetophenone, Ethylhexylglycerin, Phenoxyethanol, Chlorphenesin, Sodium Dehydroacetate, Citric Acid, Sodium Hydroxide.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ILLUMINIZING BLENDROPS BROAD SPECTRUM SPF 40
homosalate, octisalate, zinc oxide solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44717-083 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 6 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 12 g in 100 mL Inactive Ingredients Ingredient Name Strength PIDOLIC ACID (UNII: SZB83O1W42) TOCOPHEROL (UNII: R0ZB2556P8) GLUCONOLACTONE (UNII: WQ29KQ9POT) CHLORPHENESIN (UNII: I670DAL4SZ) PROPANEDIOL (UNII: 5965N8W85T) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ROSEMARY (UNII: IJ67X351P9) CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) SODIUM BENZOATE (UNII: OJ245FE5EU) RICE BRAN (UNII: R60QEP13IC) MYRISTYL ALCOHOL (UNII: V42034O9PU) POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7) PHENOXYETHANOL (UNII: HIE492ZZ3T) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T) FERRIC OXIDE RED (UNII: 1K09F3G675) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) TRANEXAMIC ACID (UNII: 6T84R30KC1) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) CETYL ALCOHOL (UNII: 936JST6JCN) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44717-083-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/02/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/02/2024 Labeler - Wasatch Product Development, LLC (962452533)