Benzoin - 46414-8888-2 - (Benzoin)

Alphabetical Index


Drug Information of Benzoin

Product NDC: 46414-8888
Proprietary Name: Benzoin
Non Proprietary Name: Benzoin
Active Ingredient(s): .12; .6; .48; .24    g/.12mL; g/.6mL; g/.48mL; g/.24mL & nbsp;   Benzoin
Administration Route(s): TOPICAL
Dosage Form(s): SWAB
Coding System: National Drug Codes(NDC)

Labeler Information of Benzoin

Product NDC: 46414-8888
Labeler Name: James Alexander Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19761025

Package Information of Benzoin

Package NDC: 46414-8888-2
Package Description: 60 mL in 1 BOX (46414-8888-2)

NDC Information of Benzoin

NDC Code 46414-8888-2
Proprietary Name Benzoin
Package Description 60 mL in 1 BOX (46414-8888-2)
Product NDC 46414-8888
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzoin
Dosage Form Name SWAB
Route Name TOPICAL
Start Marketing Date 19761025
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name James Alexander Corporation
Substance Name ALOE; BENZOIN; LIQUIDAMBAR STYRACIFLUA RESIN; TOLU BALSAM
Strength Number .12; .6; .48; .24
Strength Unit g/.12mL; g/.6mL; g/.48mL; g/.24mL
Pharmaceutical Classes

Complete Information of Benzoin


General Information