Muscle Rub

Product NDC: 52000-020
11-digit product format: 520000020
Labeler code: 52000
Product ID: 52000-020_d882ec1c-a98e-693d-e053-2995a90a282d
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: Universal Distribution Center LLC
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2015-04-15
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 0 g/g
NDC exclude flag: No
Listing certified through: 2023-12-31
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	52000-020		I	Inactivated by FDA		2026-10-05
excluded package	package	52000-020	52000-020-37	I	Inactivated by FDA		2026-10-05

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 · 8 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	52000-020-37	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	52000-020-37	`f5e01cc5f278…`	`a2eaf40c39c3…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	52000-020-37	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	52000-020-37	`9bebd1f3094a…`	`5416666fcb17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52000-020-37	2025-07-29	C162847	48780-1	9d75b9d1-200a-f424-e053-dadaa90a57ce	U Muscle Rub Gel
52000-020-37	2020-12-14	C162847	48780-1	9d75b9d1-200a-f424-e053-dadaa90a57ce	U Muscle Rub Gel
52000-020-37	2020-01-31	C162847	48780-1	9d75b9d1-200a-f424-e053-dadaa90a57ce	U Muscle Rub Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52000-020-37	Muscle Rub	1 in 1 BOX	GEL	1		4
52000-020-38	Muscle Rub	35 g in 1 TUBE	GEL	35		4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
CAMPHOR (SYNTHETIC)	INACTIVE INGREDIENT	5TJD82A1ET	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
CARBOMER 940	INACTIVE INGREDIENT	4Q93RCW27E	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
DMDM HYDANTOIN	INACTIVE INGREDIENT	BYR0546TOW	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
ISOCETETH-20	INACTIVE INGREDIENT	O020065R7Z	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
POLYOXYL 40 HYDROGENATED CASTOR OIL	INACTIVE INGREDIENT	7YC686GQ8F	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-020	MUSCLE RUB (MENTHOL) GEL [UNIVERSAL DISTRIBUTION CENTER LLC]	4	Legacy NDC, 2 package rows	20241212_4481b268-8e92-4dab-a376-98db8b360a7c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
282805	menthol 2.5 % Topical Gel	PSN	4481b268-8e92-4dab-a376-98db8b360a7c	4
282805	menthol 0.025 MG/MG Topical Gel	SCD	4481b268-8e92-4dab-a376-98db8b360a7c	4
282805	menthol 2.5 % Topical Gel	SY	4481b268-8e92-4dab-a376-98db8b360a7c	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
52000-020-37	52000002037	1 TUBE in 1 BOX (52000-020-37) > 35 g in 1 TUBE (52000-020-38)	1 tube	2020-12-13	0000-00-00	No	No	Current
52000-020-38	52000002038	35 g in 1 TUBE	35 g					Historical