Dragon Pain Relief

Product NDC
50066-410
11-digit product format
500660410
Labeler code
50066
Product ID
50066-410_e557bd5d-273e-49a0-9485-2557f5f9e230
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
GEL
Route
TOPICAL
Labeler
Genomma Lab USA
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-12
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
40 mg/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50066-410-022022-01-28C16284748780-1d6a99b39-cdde-a426-e053-dadaa90af4c2Dragon ® Pain Relief Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50066-410-02Dragon Pain Relief56.7 g in 1 TUBEGEL56.71
50066-410-02Dragon Pain Relief1 in 1 CARTONGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50066-410DRAGON PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [GENOMMA LAB USA]1Legacy NDC, 2 package rows20201210_9206462e-3bf5-4cf8-8bb3-d6de5911e5d1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN9206462e-3bf5-4cf8-8bb3-d6de5911e5d11
415974menthol 0.04 MG/MG Topical GelSCD9206462e-3bf5-4cf8-8bb3-d6de5911e5d11
415974menthol 4 % Topical GelSY9206462e-3bf5-4cf8-8bb3-d6de5911e5d11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50066-410-02500660410021 TUBE in 1 CARTON (50066-410-02) > 56.7 g in 1 TUBE1 tube2020-11-120000-00-00NoNoCurrent