Banish My Pain

Product NDC
72895-081
11-digit product format
728950081
Labeler code
72895
Product ID
72895-081_883d65e1-78a9-be9d-e053-2a95a90aa591
Type
HUMAN OTC DRUG
Nonproprietary name
Camphor
Dosage form
OINTMENT
Route
TOPICAL
Labeler
LAIDEN MONTANA EMU PRODUCTS
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-05-06
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL)
Active strength
3 g/60mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72895-081-022021-01-29C16284748780-1ba0f9c33-4545-a910-e053-dadaa90a0b85Banish My Pain

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72895-081-02Banish My Pain60 mL in 1 JAROINTMENT601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72895-081BANISH MY PAIN (CAMPHOR) OINTMENT [LAIDEN MONTANA EMU PRODUCTS]1Legacy NDC, 1 package rows20190509_883d65e1-78aa-be9d-e053-2a95a90aa591.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
72895-081-027289500810260 mL in 1 JAR60 mlHistorical