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LEADER PAIN RELIEVING RUB ULTRA - 37205-460-16 - (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE)

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Drug Information of LEADER PAIN RELIEVING RUB ULTRA

Product NDC: 37205-460
Proprietary Name: LEADER PAIN RELIEVING RUB ULTRA
Non Proprietary Name: CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Active Ingredient(s): 40; 100; 300    mg/g; mg/g; mg/g & nbsp;   CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of LEADER PAIN RELIEVING RUB ULTRA

Product NDC: 37205-460
Labeler Name: CARDINAL HEALTH
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120731

Package Information of LEADER PAIN RELIEVING RUB ULTRA

Package NDC: 37205-460-16
Package Description: 1 TUBE in 1 CARTON (37205-460-16) > 57 g in 1 TUBE

NDC Information of LEADER PAIN RELIEVING RUB ULTRA

NDC Code 37205-460-16
Proprietary Name LEADER PAIN RELIEVING RUB ULTRA
Package Description 1 TUBE in 1 CARTON (37205-460-16) > 57 g in 1 TUBE
Product NDC 37205-460
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120731
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CARDINAL HEALTH
Substance Name CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Strength Number 40; 100; 300
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of LEADER PAIN RELIEVING RUB ULTRA


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