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

  • NDC Code(s): 44717-084-01
  • Packager: Wasatch Product Development, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 1, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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

    fskdjfsd

  • 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

    Perfecting blend drops

  • INGREDIENTS AND APPEARANCE
    PERFECTING BLENDROPS BROAD SPECTRUM SPF 40 
    homosalate, octisalate, zinc oxide solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44717-084
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE12 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE6 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44717-084-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product02/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/14/2024
    Labeler - Wasatch Product Development, LLC (962452533)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!