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ZIKS ARTHRITIS PAIN RELIEF - 63044-030-60 - (ZIKS ARTHRITIS PAIN RELIEF)

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Drug Information of ZIKS ARTHRITIS PAIN RELIEF

Product NDC: 63044-030
Proprietary Name: ZIKS ARTHRITIS PAIN RELIEF
Non Proprietary Name: ZIKS ARTHRITIS PAIN RELIEF
Active Ingredient(s): .014; .566; 6.79    mg/g; mg/g; mg/g & nbsp;   ZIKS ARTHRITIS PAIN RELIEF
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ZIKS ARTHRITIS PAIN RELIEF

Product NDC: 63044-030
Labeler Name: Nnodum Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part334
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19991110

Package Information of ZIKS ARTHRITIS PAIN RELIEF

Package NDC: 63044-030-60
Package Description: 56.6 g in 1 TUBE (63044-030-60)

NDC Information of ZIKS ARTHRITIS PAIN RELIEF

NDC Code 63044-030-60
Proprietary Name ZIKS ARTHRITIS PAIN RELIEF
Package Description 56.6 g in 1 TUBE (63044-030-60)
Product NDC 63044-030
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ZIKS ARTHRITIS PAIN RELIEF
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19991110
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Nnodum Pharmaceuticals
Substance Name CAPSAICIN; MENTHOL; METHYL SALICYLATE
Strength Number .014; .566; 6.79
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of ZIKS ARTHRITIS PAIN RELIEF


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