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ATOPALM PAIN RELIEVING - 51141-0239-2 - (MENTHOL)

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Drug Information of ATOPALM PAIN RELIEVING

Product NDC: 51141-0239
Proprietary Name: ATOPALM PAIN RELIEVING
Non Proprietary Name: MENTHOL
Active Ingredient(s): 10    g/100g & nbsp;   MENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ATOPALM PAIN RELIEVING

Product NDC: 51141-0239
Labeler Name: NeoPharm Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120814

Package Information of ATOPALM PAIN RELIEVING

Package NDC: 51141-0239-2
Package Description: 1 TUBE in 1 CARTON (51141-0239-2) > 57 g in 1 TUBE

NDC Information of ATOPALM PAIN RELIEVING

NDC Code 51141-0239-2
Proprietary Name ATOPALM PAIN RELIEVING
Package Description 1 TUBE in 1 CARTON (51141-0239-2) > 57 g in 1 TUBE
Product NDC 51141-0239
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MENTHOL
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120814
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NeoPharm Co., Ltd.
Substance Name MENTHOL
Strength Number 10
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of ATOPALM PAIN RELIEVING


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