FDA.reportPublic FDA data

Sunscreen

Product NDC
79481-9926
Requested package NDC
79481-9926-1
11-digit product format
794819926
Labeler code
79481
Product ID
79481-9926_750fd1de-bf68-49ea-a3b1-7e218f198f95
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
SPRAY
Route
TOPICAL
Labeler
MEIJER
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2020-10-28
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
90 g/g; g/g; g/g; g/g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage79481-992679481-9926-1DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-9926SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [MEIJER DISTRIBUTION, INC]4Legacy NDC20250312_e2c956fb-981c-48ff-ba07-c341958f8ec6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79481-9926-179481992601156 g in 1 BOTTLE, SPRAY (79481-9926-1) 156 g2020-10-280000-00-00NoNoCurrent