Home NDC 79481-9926-3 Sunscreen
Product NDC 79481-9926
Requested package NDC 79481-9926-3
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 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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 79481-9926 79481-9926-3 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 NDC Dashboard title SPL version Validation Dashboard ZIP 79481-9926 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [MEIJER DISTRIBUTION, INC] 4 Legacy NDC 20250312_e2c956fb-981c-48ff-ba07-c341958f8ec6.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79481-9926-3 79481992603 258 g in 1 BOTTLE, SPRAY (79481-9926-3) 258 g 2020-10-28 0000-00-00 No No Current