Home NDC 11822-2055-1 sunscreen
Product NDC 11822-2055
Requested package NDC 11822-2055-1
11-digit product format 118222055
Labeler code 11822
Product ID 11822-2055_b37bd23f-8206-4707-a42f-db8f8c1c7faa
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form SPRAY
Route TOPICAL
Labeler Rite Aid
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2021-12-08
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 11822-2055 11822-2055-1 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 11822-2055 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [RITE AID] 6 Legacy NDC 20240906_fcb3eda5-fec2-41de-a87c-151cf003a3b9.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11822-2055-1 11822205501 56 g in 1 BOTTLE, SPRAY (11822-2055-1) 56 g 2021-12-08 0000-00-00 No No Current