Muscle Rub

Product NDC: 29500-2433
11-digit product format: 295002433
Labeler code: 29500
Product ID: 29500-2433_8d9b88cc-7bb7-4532-9a07-201713581ea0
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: CREAM
Route: TOPICAL
Labeler: Personal Care Products, Inc.
Application: part348
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2013-07-10
Marketing end: 0000-00-00
Substance: MENTHOL
Active strength: 1 g/42g
NDC exclude flag: No
Listing certified through: 2019-12-31
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	29500-2433		I	Inactivated by FDA		2026-10-05
excluded package	package	29500-2433	29500-2433-1	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 · 42 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	29500-2433-1	`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	29500-2433-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	29500-2433-1	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	29500-2433-1	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	29500-2433-1	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	29500-2433-1	`cdf11ea48f46…`	`ba0047e9e063…`
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	29500-2433-1	`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	29500-2433-1	`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	29500-2433-1	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	29500-2433-1	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	29500-2433-1	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	29500-2433-1	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	29500-2433-1	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	29500-2433-1	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	29500-2433-1	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	29500-2433-1	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	29500-2433-1	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	29500-2433-1	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	29500-2433-1	`8dfbde2a14a4…`	`c9ff85d89658…`
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	29500-2433-1	`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	29500-2433-1	`9bebd1f3094a…`	`5416666fcb17…`

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
29500-2433-1	2020-01-31	C162847	48780-1	9d75b9d0-c2a7-f424-e053-dadaa90a57ce	a9d57473-530f-4fc1-979c-28dc82d7c32f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
29500-2433-1	Muscle RubUltra Strength Pain Relieving	42 g in 1 TUBE	CREAM	42		1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
CAMPHOR (NATURAL)	INACTIVE INGREDIENT	N20HL7Q941	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)	INACTIVE INGREDIENT	4Q93RCW27E	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
DMDM HYDANTOIN	INACTIVE INGREDIENT	BYR0546TOW	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
GLYCERYL MONOSTEARATE	INACTIVE INGREDIENT	230OU9XXE4	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
POLYOXYL 40 HYDROGENATED CASTOR OIL	INACTIVE INGREDIENT	7YC686GQ8F	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
29500-2433	MUSCLE RUB ULTRA STRENGTH PAIN RELIEVING (MENTHOL) CREAM [PERSONAL CARE PRODUCTS, INC.]	1	Legacy NDC, 1 package rows	20130725_a9d57473-530f-4fc1-979c-28dc82d7c32f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1291226	menthol 2.5 % Topical Cream	PSN	a9d57473-530f-4fc1-979c-28dc82d7c32f	1
1291226	menthol 25 MG/ML Topical Cream	SCD	a9d57473-530f-4fc1-979c-28dc82d7c32f	1
1291226	menthol 2.5 % Topical Cream	SY	a9d57473-530f-4fc1-979c-28dc82d7c32f	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
29500-2433-1	29500243301	42 g in 1 TUBE	42 g	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
MENTHOL - Personal Care Products, Inc. \| Anicare Pharmaceuticals Pvt. Ltd.	Personal Care Products, Inc. \| Anicare Pharmaceuticals Pvt. Ltd.	2013-07-10	HUMAN OTC DRUG LABEL	1