Chondro-Pro

Product NDC
68393-349
11-digit product format
683930349
Labeler code
68393
Product ID
68393-349_639dbf42-6c4b-413c-a24a-110c63c48de3
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
GEL
Route
TOPICAL
Labeler
MDR Fitness Corp.
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-03-04
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
1 mg/100mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68393-349-022021-01-29C16284748780-1ba0f9c33-2b2a-a910-e053-dadaa90a0b85Chondro-Pro™ Pain Relief Roll On

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68393-349-02Chondro-Pro Pain Relief Roll On59.1 mL in 1 BOTTLE, DISPENSINGGEL59.12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68393-349CHONDRO-PRO PAIN RELIEF ROLL ON (MENTHOL, UNSPECIFIED FORM) GEL [MDR FITNESS CORP.]2Legacy NDC, 1 package rows20191228_a4a42692-5721-425b-9234-0b775b77bbf2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
68393-349-026839303490259.1 mL in 1 BOTTLE, DISPENSING59.1 mlHistorical