FDA.reportPublic FDA data

Sunscreen

Product NDC
11822-0714
11-digit product format
118220714
Labeler code
11822
Product ID
11822-0714_b164a3fe-4df6-4bc3-90b7-f03aab024e1c
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Rite Aid
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-12-02
Marketing end
0000-00-00
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30 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 productproduct11822-0714DDiscontinued by firm2026-10-12
excluded packagepackage11822-071411822-0714-3DDiscontinued by firm2026-10-12

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
11822-0714SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [RITE AID]5Legacy NDC20240927_a9f9ca00-47ba-4aa5-9bf9-7a01daba88b4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0714-311822071403236 mL in 1 BOTTLE, PLASTIC (11822-0714-3) 236 ml2021-12-020000-00-00NoNoCurrent