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

Additional Listing Data#

Finished product
Yes
Brand name base
Green Compass Reduce Roll-On Pain Relief

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73132-003-602025-02-01C16284748780-12cef2736-8b55-d83d-e063-dadaa90ab31fGreen Compass Reduce Roll-On Pain Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73132-003-60Green Compass Reduce Roll-On Pain Relief60 mL in 1 BOTTLE, WITH APPLICATORLIQUID603
73132-003-60Green Compass Reduce Roll-On Pain Relief1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73132-003GREEN COMPASS REDUCE ROLL-ON PAIN RELIEF (MENTHOL) LIQUID [GREEN COMPASS, INC.]3Current NDC, Legacy NDC, 2 package rows20250131_b5916aa2-428c-5637-e053-2995a90a08b0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73132-003-60731320003601 BOTTLE, WITH APPLICATOR in 1 CARTON (73132-003-60) / 60 mL in 1 BOTTLE, WITH APPLICATOR2020-12-032026-10-22NoNoCurrent