FDA.reportPublic FDA data

Sunscreen

Product NDC
79481-9926
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct79481-9926DDiscontinued by firm2026-10-12
excluded packagepackage79481-992679481-9926-1DDiscontinued by firm2026-10-12
excluded packagepackage79481-992679481-9926-2DDiscontinued by firm2026-10-12
excluded packagepackage79481-992679481-9926-3DDiscontinued by firm2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-0579481-9926-2d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0579481-9926-3d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2679481-9926-2f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3179481-9926-22ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2879481-9926-2a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2179481-9926-2cfe11265f3b6…090c488252e2…

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
79481-9926-279481992602236 g in 1 BOTTLE, SPRAY (79481-9926-2) 236 g2020-10-280000-00-00NoNoCurrent
79481-9926-379481992603258 g in 1 BOTTLE, SPRAY (79481-9926-3) 258 g2020-10-280000-00-00NoNoCurrent