Home NDC 73132-005 Green Compass Reduce Pain Relief with Menthol
Product NDC 73132-005
11-digit product format 731320005
Labeler code 73132
Product ID 73132-005_2c7baad3-2add-ba3f-e063-6294a90a3bb3
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler Green Compass, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-11-01
Substance MENTHOL, UNSPECIFIED FORM
Active strength 5 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 2025-01-20 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 73132-005-60 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 73132-005-00 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 73132-005-60 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 73132-005-00 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 Pain Relief with Menthol
Listing expiration 2026-12-31 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73132-005-00 Green Compass Reduce Pain Relief with Menthol 2 mL in 1 PACKET GEL 2 2 73132-005-60 Green Compass Reduce Pain Relief with Menthol 60 mL in 1 BOTTLE, WITH APPLICATOR GEL 60 2 73132-005-60 Green Compass Reduce Pain Relief with Menthol 1 in 1 CARTON GEL 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73132-005 GREEN COMPASS REDUCE PAIN RELIEF WITH MENTHOL (MENTHOL) GEL [GREEN COMPASS, INC.] 2 Current NDC, 3 package rows 20250126_0a0c212e-ae5d-8505-e063-6394a90af622.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 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73132-005-00 73132000500 2 mL in 1 PACKET (73132-005-00) 2 ml 2023-11-01 Yes No Current 73132-005-60 73132000560 1 BOTTLE, WITH APPLICATOR in 1 CARTON (73132-005-60) / 60 mL in 1 BOTTLE, WITH APPLICATOR 2023-11-01 No No Current