ARCTIC RELIEF ROLL ON

Product NDC
58980-617
11-digit product format
589800617
Labeler code
58980
Product ID
58980-617_3dbca047-fc59-41a1-a742-832f889bb4ce
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM
Dosage form
GEL
Route
TOPICAL
Labeler
STRATUS PHARMACEUTICALS INC
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-09-15
Marketing end
0000-00-00
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
4 g/90g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58980-617-312021-02-24C16284748780-19d75b9d0-e4c1-f424-e053-dadaa90a57cedb2ebe1b-e333-45c2-9009-2f89437dd4f3
58980-617-312020-01-31C16284748780-19d75b9d0-e4c1-f424-e053-dadaa90a57cedb2ebe1b-e333-45c2-9009-2f89437dd4f3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58980-617-31GM - Gram58980-617f5ca706b-0fe4-4ab0-8896-b2dad89ebbfb12018-10-11