NDC 61600-052 - MYOGESIC-CS VETGENIX

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 61600-052
Package NDCs from labels: 61600-052-16, 61600-052-04, 61600-052-32, 61600-052-64, 61600-052-38
Manufacturer: VETGENIX
Effective date: 2011-02-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
MYOGESIC-CS VETGENIX - VETGENIX	VETGENIX	2011-02-08	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61600-052-04	MYOGESIC-CSVETGENIX	113 g in 1 BOTTLE, SPRAY	SPRAY	113	1
61600-052-16	MYOGESIC-CSVETGENIX	452 g in 1 BOTTLE, SPRAY	SPRAY	452	1
61600-052-32	MYOGESIC-CSVETGENIX	904 g in 1 BOTTLE, SPRAY	SPRAY	904	1
61600-052-38	MYOGESIC-CSVETGENIX	3616 g in 1 JUG	SPRAY	3616	1
61600-052-64	MYOGESIC-CSVETGENIX	1808 g in 1 JUG	SPRAY	1808	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61600-052	MYOGESIC-CS VETGENIX (MENTHOL AND PRAMOXINE HYDROCHLORIDE) SPRAY [VETGENIX]	1	5 package rows	20111004_e65d8f43-3f4d-4694-8bad-06c482fe97ff.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	MYOGESIC-CS VETGENIX (MENTHOL AND PRAMOXINE HYDROCHLORIDE) SPRAY [VETGENIX]	1
pramoxine hydrochloride	ACTIVE INGREDIENT	88AYB867L5	MYOGESIC-CS VETGENIX (MENTHOL AND PRAMOXINE HYDROCHLORIDE) SPRAY [VETGENIX]	1
menthol	ACTIVE MOIETY	L7T10EIP3A	MYOGESIC-CS VETGENIX (MENTHOL AND PRAMOXINE HYDROCHLORIDE) SPRAY [VETGENIX]	1
pramoxine	ACTIVE MOIETY	068X84E056	MYOGESIC-CS VETGENIX (MENTHOL AND PRAMOXINE HYDROCHLORIDE) SPRAY [VETGENIX]	1

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 125 of 125 · 2,487 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Sore Muscle Rub Vanishing Scent	MENTHOL	CVS Pharmacy	454bbde9-3076-6977-e054-00144ff88e88	2017-01-04	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare Turbo	MENTHOL, CAMPHOR	Active and Innovative Inc.	42f1e14a-3ac6-01c1-e054-00144ff8d46c	2016-12-05	Warnings	Exact identifier unii: L7T10EIP3A
Dr. Blue	MENTHOL	Indiana Botanic Gardens	1b1150bd-e087-4d8f-b0d6-0d935cf6e31e	2016-11-01	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare	CAMPHOR, MENTHOL	Active and Innovative Inc.	1ec95bbb-cd7d-2588-e054-00144ff8d46c	2016-08-11	Warnings	Exact identifier unii: L7T10EIP3A
Professional Therapy MuscleCare pain relieving gel Extra Strength	CAMPHOR, MENTHOL	Active and Innovative Inc.	1d2403d9-99c3-24f5-e054-00144ff8d46c	2016-08-10	Warnings	Exact identifier unii: L7T10EIP3A
MED AID CHEST RUB	MENTHOL AND CAMPHOR AND EUCALYPTUS OIL	Blue Cross Laboratories, Inc.	429041fe-55a5-4df1-b60d-721103e5c65e	2016-07-27	Warnings	Exact identifier unii: L7T10EIP3A
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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