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HARMON Extra Strength Pain Relieving Roll-On - 63940-150-03 - (MENTHOL)

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Drug Information of HARMON Extra Strength Pain Relieving Roll-On

Product NDC: 63940-150
Proprietary Name: HARMON Extra Strength Pain Relieving Roll-On
Non Proprietary Name: MENTHOL
Active Ingredient(s): 3.5    mL/100mL & nbsp;   MENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of HARMON Extra Strength Pain Relieving Roll-On

Product NDC: 63940-150
Labeler Name: Harmon Stores Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120905

Package Information of HARMON Extra Strength Pain Relieving Roll-On

Package NDC: 63940-150-03
Package Description: 89 mL in 1 BOTTLE, WITH APPLICATOR (63940-150-03)

NDC Information of HARMON Extra Strength Pain Relieving Roll-On

NDC Code 63940-150-03
Proprietary Name HARMON Extra Strength Pain Relieving Roll-On
Package Description 89 mL in 1 BOTTLE, WITH APPLICATOR (63940-150-03)
Product NDC 63940-150
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MENTHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120905
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Harmon Stores Inc.
Substance Name MENTHOL
Strength Number 3.5
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of HARMON Extra Strength Pain Relieving Roll-On


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