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Ice Cold Analgesic Gel - 52000-013-18 - (Menthol and Camphor)

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Drug Information of Ice Cold Analgesic Gel

Product NDC: 52000-013
Proprietary Name: Ice Cold Analgesic Gel
Non Proprietary Name: Menthol and Camphor
Active Ingredient(s): .5; 1    g/100g; g/100g & nbsp;   Menthol and Camphor
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Ice Cold Analgesic Gel

Product NDC: 52000-013
Labeler Name: Universal Distribution Center LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130315

Package Information of Ice Cold Analgesic Gel

Package NDC: 52000-013-18
Package Description: 170 g in 1 TUBE (52000-013-18)

NDC Information of Ice Cold Analgesic Gel

NDC Code 52000-013-18
Proprietary Name Ice Cold Analgesic Gel
Package Description 170 g in 1 TUBE (52000-013-18)
Product NDC 52000-013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol and Camphor
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20130315
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Universal Distribution Center LLC
Substance Name CAMPHOR (SYNTHETIC); MENTHOL
Strength Number .5; 1
Strength Unit g/100g; g/100g
Pharmaceutical Classes

Complete Information of Ice Cold Analgesic Gel


General Information