Home NDC 33992-1136 Assured
Product NDC 33992-1136
11-digit product format 339921136
Labeler code 33992
Product ID 33992-1136_d85735b7-7a77-42df-8fb1-9fefb8aaa791
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler Greenbrier International, Inc.
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2012-05-15
Marketing end 0000-00-00
Substance MENTHOL, UNSPECIFIED FORM
Active strength 3 g/100g
NDC exclude flag No
Listing certified through 2020-12-31
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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 33992-1136-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 33992-1136-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 33992-1136-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 33992-1136-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 33992-1136-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 33992-1136-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 33992-1136-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 33992-1136-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 33992-1136-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 33992-1136-1 AssuredMuscle Rub 42.5 g in 1 TUBE GEL 42.5 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MENTHOL ACTIVE INGREDIENT L7T10EIP3A ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 MENTHOL ACTIVE MOIETY L7T10EIP3A ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 CAMPHOR (SYNTHETIC) INACTIVE INGREDIENT 5TJD82A1ET ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 DMDM HYDANTOIN INACTIVE INGREDIENT BYR0546TOW ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 ISOPROPYL ALCOHOL INACTIVE INGREDIENT ND2M416302 ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 POLYOXYL 40 HYDROGENATED CASTOR OIL INACTIVE INGREDIENT 7YC686GQ8F ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 33992-1136 ASSURED MUSCLE RUB (MENTHOL) GEL [GREENBRIER INTERNATIONAL, INC.] 3 Legacy NDC, 1 package rows 20171229_81317756-e678-40fa-95ea-a9d7ecd98481.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 33992-1136-1 33992113601 42.5 g in 1 TUBE (33992-1136-1) 42.5 g 2012-05-15 0000-00-00 No No Current