FDA.reportPublic FDA data

Sunscreen

Product NDC
79481-0914
11-digit product format
794810914
Labeler code
79481
Product ID
79481-0914_0ebb7964-0479-40cb-a5e4-9a95d7209976
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Meijer
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-03-15
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
90 mg/mL; mg/mL; mg/mL; mg/mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct79481-0914DDiscontinued by firm2026-10-15
excluded packagepackage79481-091479481-0914-2DDiscontinued 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
79481-0914SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [MEIJER DISTRIBUTION, INC]5Legacy NDC20250416_512ddf79-1405-423d-b7de-d2b73a857d4b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79481-0914-27948109140289 mL in 1 TUBE (79481-0914-2) 89 ml2021-03-150000-00-00NoNoCurrent