HashtagSUN SPF 50 SunScreen Dabber

Product NDC
72667-017
Requested package NDC
72667-017-01
11-digit product format
726670017
Labeler code
72667
Product ID
72667-017_d31ede18-7740-a8be-e053-2a95a90aba59
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Humosalate, Octisalate, Octocrylene
Dosage form
SPONGE
Route
TOPICAL
Labeler
Inspec Solutions
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-01-29
Marketing end
0000-00-00
Substance
HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Active strength
15 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 13 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-288af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…

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
72667-017-012023-01-30C16284748780-19d75b9d0-9925-f424-e053-dadaa90a57ceMyDerm Sunscreen SPF 50

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72667-017HASHTAGSUN SPF 50 SUNSCREEN DABBER (AVOBENZONE, HUMOSALATE, OCTISALATE, OCTOCRYLENE) SPONGE [INSPEC SOLUTIONS]4Legacy NDC20211215_7bd0ce88-8158-6e53-e053-2991aa0a6236.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72667-017-017266700170119 mL in 1 BOTTLE, PLASTIC (72667-017-01) 19 ml2021-01-290000-00-00NoNoCurrent