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

Bronzing Blendrops Broad Spectrum SPF 40 by

Drug Labeling and Warnings

Bronzing 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 Ingredients
Homosalate 6%

Octisalate 5%

Zinc Oxide 12 %

Purpose

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 caused by the sun

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

INDICATIONS & USAGE

• Stop use and ask a doctor if rash occurs.

WARNINGS

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 before 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 skin aging. To decrease this risk, regularly use a sunscreen
with broad spectrum SPF 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-sleeve shirts, pants, hats, and sunglasse. Children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

Other information

Protect this product from excessive heat and direct sun

INACTIVE INGREDIENT

Water, Butyloctyl Salicylate, C12-15 Alkyl Benozate, Mica, Propanediol, Coco-Caprylate/Caprate, Polyglyceryl-6 Stearate, Carthamus Tinctorius (Safflower) Oleosomes, Titanium Dioxide (CI77891), Iron Oxides (CI 77491), Tranexamic Acid, PCA, Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Oryza Sativa (Rice) Bran Extract, Helianthus Annuus (Sunflower) Extract, Tocopherol, Gluconolactone, Polyglutamic Acid, Theobroma Cacao (Cocoa) Extract, Carthamus Tinctorius (Safflower) Seedcake Extract, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyhydroxystearic Acid, Cetyl Alcohol, Isopropyl Titanium Triisostearate, Polyglyceryl-6 Behenate, Iron Oxides (CI 77499), Myristyl Alcohol, Sorbitan Isostearate, 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

Bronzing Blendrops

Broad Spectrum SPF 40

Oil Control Sun-kissed Finish Priming Drops

1 fl. oz. / 30 ml

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44717-082
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	12 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
TOCOPHEROL (UNII: R0ZB2556P8)
MICA (UNII: V8A1AW0880)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ROSEMARY (UNII: IJ67X351P9)
RICE BRAN (UNII: R60QEP13IC)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)
TRANEXAMIC ACID (UNII: 6T84R30KC1)
CETYL ALCOHOL (UNII: 936JST6JCN)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
COCOA (UNII: D9108TZ9KG)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)
PROPANEDIOL (UNII: 5965N8W85T)
PIDOLIC ACID (UNII: SZB83O1W42)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44717-082-01	30 mL in 1 BOTTLE, PLASTIC; 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)