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PROTOXIN

Medically reviewed by Drugs.com. Last updated on Nov 1, 2021.

Dosage form: gel
Ingredients: CLOSTRIDIUM BOTULINUM 10g in 10mL
Labeler: PROTOX Inc.
NDC Code: 71066-0001

Clostridium botulinum Toxin Type A

Normal human serum albumin, Sodium chloride

Stop a secretion of the neurotransmitter acetylcholine in a place to see nerves and muscles.
Lessening the rigidity of the child with cerebral palsy using the qualities that lead to muscle paralysis.

Keep out of reach of children.

Confirm the validity of the product label

to make sure the sterilizatios is not damaged before using

N/A

N/A

PROTOXIN 
clostridium botulinum toxin type a gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71066-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CLOSTRIDIUM BOTULINUM (CLOSTRIDIUM BOTULINUM) CLOSTRIDIUM BOTULINUM10 g  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ALBUMIN HUMAN 
SODIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:71066-0001-110 mL in 1 VIAL
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/10/2016
Labeler - PROTOX Inc. (689846300)
Registrant - PROTOX Inc. (689846300)
Establishment
NameAddressID/FEIOperations
PROTOX Inc.689846300manufacture(71066-0001)

Document Id: 41280d2a-9232-5800-e054-00144ff88e88
Set id: 41280d2a-9231-5800-e054-00144ff88e88
Version: 1
Effective Time: 20161110
 
PROTOX Inc.

Further information

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