ARCTIC RELIEF PAIN RELIEVING

Product NDC
58980-618
11-digit product format
589800618
Labeler code
58980
Product ID
58980-618_5f5133d0-e870-44ea-b7d6-cac8ab9e7f75
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
GEL
Route
TOPICAL
Labeler
STRATUS PHARMACEUTICALS INC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-06-07
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
5 g/113.4g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58980-618-3258980061832907.2 g in 1 BOTTLE, PUMP (58980-618-32) 907.2 g2021-06-070000-00-00NoNoCurrent
58980-618-40589800618401 TUBE in 1 BOX (58980-618-40) > 113.4 g in 1 TUBE1 tube2021-06-070000-00-00NoNoCurrent