Green Compass Reduce Roll-On Pain Relief

Product NDC: 73132-003
11-digit product format: 731320003
Labeler code: 73132
Product ID: 73132-003_f1f0305f-0054-08ad-e053-2995a90aa371
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: LIQUID
Route: TOPICAL
Labeler: Green Compass, Inc.
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2020-12-03
Marketing end: 0000-00-00
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 5 g/100mL
NDC exclude flag: No
Listing certified through: 2024-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	73132-003		D	Discontinued by firm		2026-11-03
excluded package	package	73132-003	73132-003-60	D	Discontinued by firm		2026-11-03

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.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73132-003-60	2025-02-01	C162847	48780-1	2cef2736-8b55-d83d-e063-dadaa90ab31f	Green Compass Reduce Roll-On Pain Relief

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	Legacy NDC, 2 package rows	20250131_b5916aa2-428c-5637-e053-2995a90a08b0.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

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	0000-00-00	No	No	Current