Keralyt - 11086-030-41 - (salicylic acid)

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Drug Information of Keralyt

Product NDC: 11086-030
Proprietary Name: Keralyt
Non Proprietary Name: salicylic acid
Active Ingredient(s): 6    g/100g & nbsp;   salicylic acid
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Keralyt

Product NDC: 11086-030
Labeler Name: Summers Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091101

Package Information of Keralyt

Package NDC: 11086-030-41
Package Description: 1 TUBE in 1 PACKAGE (11086-030-41) > 40 g in 1 TUBE (11086-030-40)

NDC Information of Keralyt

NDC Code 11086-030-41
Proprietary Name Keralyt
Package Description 1 TUBE in 1 PACKAGE (11086-030-41) > 40 g in 1 TUBE (11086-030-40)
Product NDC 11086-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name salicylic acid
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20091101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Summers Laboratories Inc
Substance Name SALICYLIC ACID
Strength Number 6
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Keralyt


General Information