Pain Relieving

Product NDC
37205-824
11-digit product format
372050824
Labeler code
37205
Product ID
37205-824_93f93142-2b32-4589-904d-48290c2622e0
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
Cardinal Health
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-01-18
Marketing end
2024-12-31
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
35 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-824-26ML - Milliliter37205-8244142dd58-dea8-439c-81de-63ee1fc8512612012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37205-824-26372050824261 BOTTLE in 1 CARTON (37205-824-26) > 118 mL in 1 BOTTLE1 bottle2012-01-182024-12-31NoNoCurrent