Home NDC 61577-3221-5 SOMBRA COOL THERAPY
Product NDC 61577-3221
Requested package NDC 61577-3221-5
11-digit product format 615773221
Labeler code 61577
Product ID 61577-3221_5fe37a57-1a13-4f93-af5a-9c1899c2c066
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form GEL
Route TOPICAL
Labeler SOMBRA COSMETICS INC.
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2022-05-17
Marketing end 0000-00-00
Substance MENTHOL
Active strength 0 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 2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 61577-3221 61577-3221-5 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61577-3221 SOMBRA COOL THERAPY (MENTHOL) GEL [SOMBRA COSMETICS INC.] 8 Legacy NDC 20250529_87e9b16b-1cab-48f7-b9e4-1c3eaeeb3ca3.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61577-3221-5 61577322105 85 g in 1 BOTTLE, PLASTIC (61577-3221-5) 85 g 2016-05-21 0000-00-00 No No Current