Home NDC 73132-003 Green Compass Reduce Roll-On Pain Relief
Product NDC 73132-003
11-digit product format 731320003
Labeler code 73132
Product ID 73132-003_2c7bc7eb-b086-ef56-e063-6394a90a6f42
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form LIQUID
Route TOPICAL
Labeler Green Compass, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-03
Marketing end 2026-10-22
Substance MENTHOL, UNSPECIFIED FORM
Active strength 5 g/100mL
NDC exclude flag No
Current FDA listing Yes 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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 73132-003-60 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 73132-003-60 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73132-003-60 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Green Compass Reduce Roll-On Pain Relief Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73132-003-60 Green Compass Reduce Roll-On Pain Relief 60 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 60 3 73132-003-60 Green Compass Reduce Roll-On Pain Relief 1 in 1 CARTON LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73132-003 GREEN COMPASS REDUCE ROLL-ON PAIN RELIEF (MENTHOL) LIQUID [GREEN COMPASS, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20250131_b5916aa2-428c-5637-e053-2995a90a08b0.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 73132-003-60 73132000360 1 BOTTLE, WITH APPLICATOR in 1 CARTON (73132-003-60) / 60 mL in 1 BOTTLE, WITH APPLICATOR 2020-12-03 2026-10-22 No No Current