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up and up pain relief - 11673-136-01 - (menthol, methyl salicylate)

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Drug Information of up and up pain relief

Product NDC: 11673-136
Proprietary Name: up and up pain relief
Non Proprietary Name: menthol, methyl salicylate
Active Ingredient(s): 100; 300    mg/g; mg/g & nbsp;   menthol, methyl salicylate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of up and up pain relief

Product NDC: 11673-136
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080514

Package Information of up and up pain relief

Package NDC: 11673-136-01
Package Description: 1 TUBE in 1 CARTON (11673-136-01) > 85 g in 1 TUBE

NDC Information of up and up pain relief

NDC Code 11673-136-01
Proprietary Name up and up pain relief
Package Description 1 TUBE in 1 CARTON (11673-136-01) > 85 g in 1 TUBE
Product NDC 11673-136
Product Type Name HUMAN OTC DRUG
Non Proprietary Name menthol, methyl salicylate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20080514
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Target Corporation
Substance Name MENTHOL; METHYL SALICYLATE
Strength Number 100; 300
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of up and up pain relief


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