Home NDC 79753-106 COOLA SunBlur Primer SPF 50
Product NDC 79753-106
11-digit product format 797530106
Labeler code 79753
Product ID 79753-106_4c6439e8-abdb-663a-e063-6394a90ac43b
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler COOLA LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-01
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Active strength 70; 90; 30; 50 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 COOLA SunBlur Primer SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 70 mg/mL OCTOCRYLENE 90 mg/mL AVOBENZONE 30 mg/mL OCTISALATE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79753-106-01 COOLA SunBlur Primer SPF 50 30 mL in 1 BOTTLE, PUMP LOTION 30 1 79753-106-01 COOLA SunBlur Primer SPF 50 1 in 1 CARTON LOTION 1 1
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 Marketing start Sample Exclude flag Status 79753-106-01 79753010601 1 BOTTLE, PUMP in 1 CARTON (79753-106-01) / 30 mL in 1 BOTTLE, PUMP 2026-02-01 No No Current