Cold Spot - 65121-001-16 - (menthol)

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Drug Information of Cold Spot

Product NDC: 65121-001
Proprietary Name: Cold Spot
Non Proprietary Name: menthol
Active Ingredient(s): .46    L/3.8L & nbsp;   menthol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Cold Spot

Product NDC: 65121-001
Labeler Name: Pure Source
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100824

Package Information of Cold Spot

Package NDC: 65121-001-16
Package Description: 480 mL in 1 CONTAINER (65121-001-16)

NDC Information of Cold Spot

NDC Code 65121-001-16
Proprietary Name Cold Spot
Package Description 480 mL in 1 CONTAINER (65121-001-16)
Product NDC 65121-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name menthol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100824
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Pure Source
Substance Name MENTHOL
Strength Number .46
Strength Unit L/3.8L
Pharmaceutical Classes

Complete Information of Cold Spot


General Information