ILLUMINIZING BLENDROPS BROAD SPECTRUM SPF 40- homosalate, octisalate, zinc oxide solution/ drops

Illuminizing Blendrops Broad Spectrum SPF 40 by

Drug Labeling and Warnings

Illuminizing Blendrops Broad Spectrum SPF 40 by is a Otc medication manufactured, distributed, or labeled by Wasatch Product Development, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active IngredientsPurpose

Homosalate 6%, Octisalate 5%, Zinc Oxide 12% ............ Sunscreen

PURPOSE

Uses

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging casued by the sun.

KEEP OUT OF REACH OF CHILDREN

Warnings

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove.

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

Other information

Protect this product from excessive heat and direct sun.

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

Questions or Comments? 1-877-945-5274

PRINCIPAL DISPLAY PANEL

ILLUMINIZING BLENDROPS

Broad Spectrum SPF 40

Oil Control Radiant Finish Priming Drops

With Color-Correcting Tranexamic Complex

1 fl. oz/30 ml e

INGREDIENTS AND APPEARANCE

ILLUMINIZING BLENDROPS BROAD SPECTRUM SPF 40 
homosalate, octisalate, zinc oxide solution/ drops

Product 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)