NDC 71066-0001

PROTOXIN

Clostridium Botulinum Toxin Type A

PROTOXIN is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Protox Inc.. The primary component is Clostridium Botulinum.

Product ID71066-0001_41280d2a-9232-5800-e054-00144ff88e88
NDC71066-0001
Product TypeHuman Otc Drug
Proprietary NamePROTOXIN
Generic NameClostridium Botulinum Toxin Type A
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2016-11-10
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NamePROTOX Inc.
Substance NameCLOSTRIDIUM BOTULINUM
Active Ingredient Strength10 g/10mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 71066-0001-1

10 mL in 1 VIAL (71066-0001-1)
Marketing Start Date2016-11-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71066-0001-1 [71066000101]

PROTOXIN GEL
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-10
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CLOSTRIDIUM BOTULINUM10 g/10mL

OpenFDA Data

SPL SET ID:41280d2a-9231-5800-e054-00144ff88e88
Manufacturer
UNII

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