FDA.reportPublic FDA data

PHOTO-AGE SUNSCREEN

Product NDC
62551-213
Requested package NDC
62551-213-52
11-digit product format
625510213
Labeler code
62551
Product ID
62551-213_f219c41d-a661-2360-e053-2995a90a8e56
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Dosage form
GEL
Route
TOPICAL
Labeler
ADVANCED AESTHETICS
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-08-12
Marketing end
0000-00-00
Substance
OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE
Active strength
8 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2024-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage62551-21362551-213-52IInactivated by FDA2026-10-12

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 · 9 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62551-213-522025-01-30C16284748780-12cef2736-6996-d83d-e063-dadaa90ab31fADV AESTHETICS - GLYMEDPLUS MASTER AESTHETICS ELITE PHOTO-AGE SUNSCREEN SPF 30+ (62551-213)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62551-213-12PHOTO-AGE SUNSCREENSPF 3056 mL in 1 TUBEGEL563
62551-213-52PHOTO-AGE SUNSCREENSPF 301 in 1 BOXGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62551-213PHOTO-AGE SUNSCREEN SPF 30 (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) GEL [ADVANCED AESTHETICS]3Legacy NDC, 2 package rows20230113_8ebaf67f-33f1-4f32-9d8f-7e51bec35e75.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62551-213-52625510213521 TUBE in 1 BOX (62551-213-52) > 56 mL in 1 TUBE (62551-213-12) 1 tube2021-08-120000-00-00NoNoCurrent