Home NDC 44717-084 Perfecting Blendrops Broad Spectrum SPF 40
Product NDC 44717-084
11-digit product format 447170084
Labeler code 44717
Product ID 44717-084_458af489-829e-909d-e063-6294a90a3765
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Zinc Oxide
Dosage form SOLUTION/ DROPS
Route TOPICAL
Labeler Wasatch Product Development, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-14
Marketing end 2027-02-28
Substance ZINC OXIDE; HOMOSALATE; OCTISALATE
Active strength 12; 6; 5 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Perfecting Blendrops Broad Spectrum SPF 40 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 12 g/100mL HOMOSALATE 6 g/100mL OCTISALATE 5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44717-084-01 Perfecting Blendrops Broad Spectrum SPF 40 30 mL in 1 BOTTLE SOLUTION/ DROPS 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44717-084 PERFECTING BLENDROPS BROAD SPECTRUM SPF 40 (HOMOSALATE, OCTISALATE, ZINC OXIDE) SOLUTION/ DROPS [WASATCH PRODUCT DEVELOPMENT, LLC] 2 Current NDC, 1 package rows 20240302_12512cac-652e-b138-e063-6394a90ad1f2.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44717-084-01 44717008401 30 mL in 1 BOTTLE (44717-084-01) 30 ml 2024-02-14 2027-02-28 No No Historical