ecolyptus pain relieving muscle rub

Product NDC
65121-715
11-digit product format
651210715
Labeler code
65121
Product ID
65121-715_482e2384-efc5-01c7-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
Pure Source, LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-02-06
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
60 mg/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65121-715-88651210715881 TUBE in 1 CARTON (65121-715-88) > 88.7 mL in 1 TUBE1 tube2017-02-090000-00-00NoNoCurrent