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

Perfecting Blendrops Broad Spectrum SPF 40 by

Drug Labeling and Warnings

Perfecting 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 Purpose

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

PURPOSE

Uses

• Helps prevent sunburn.
• If used as directed with other sun protection measures (see Directions), drecreases 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 immediately.

INDICATIONS & USAGE

Stop use and ask a doctor if rash occurs.

WARNINGS

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DOSAGE & ADMINISTRATION

Directions

Shake well and apply liberally 15 minutes prior to sun exposure. Reapply after swimmng 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, regularly 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 sleeve shirts, pants, and sunglases. 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, 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, Polyglyceryl-6 Behenate, Iron Oxides (CI 77492), Myristyl Alcohol, Sorbitan Isostearate, Iron Oxides (CI 77491), Iron Oxides (CI 77499), Sodium Benzoate, 1,2-Hexanediol, Caprylyl Glycol, Triethoxycaprylylsilane, Caprylhydroxamic Acid, Hydroxyacetophenone, Ethylhexylglycerin, Phenoxyethanol, Chlorphenesin, Sodium Dehydroacetate, Citric Acid, Sodium Hydroxide.

QUESTIONS

Question or comments? 1-877-945-5274

PRINCIPAL DISPLAY PANEL

PERFECTING

BEAUTYBIO

PERFECTING BLENDROPS

Broad Spectrum SPF 40

Oil Control Invisible Finish Priming Drops

With Color-Correcting Tranexamic Complex

1 fl. oz./ 30 ml

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44717-084
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
RICE BRAN (UNII: R60QEP13IC)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
CHLORPHENESIN (UNII: I670DAL4SZ)
WATER (UNII: 059QF0KO0R)
ROSEMARY (UNII: IJ67X351P9)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
TOCOPHEROL (UNII: R0ZB2556P8)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
CARTHAMUS TINCTORIUS SEEDCAKE (UNII: DHQ13F4N2W)
CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
PIDOLIC ACID (UNII: SZB83O1W42)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
CETYL ALCOHOL (UNII: 936JST6JCN)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
POLYGLYCERYL-6 BEHENATE (UNII: 4T2L7QI313)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
TRANEXAMIC ACID (UNII: 6T84R30KC1)
POLYGLYCERYL-6 STEARATE (UNII: ETY9Q81E2T)
POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44717-084-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/14/2024

Labeler - Wasatch Product Development, LLC (962452533)