PROTOXIN

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

Medically reviewed by Drugs.com. Last updated on Oct 31, 2023.

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

PROTOXIN
clostridium botulinum toxin type a gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71066-0001
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CLOSTRIDIUM BOTULINUM (CLOSTRIDIUM BOTULINUM)	CLOSTRIDIUM BOTULINUM	10 g in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ALBUMIN HUMAN
SODIUM CHLORIDE

Packaging
#	Item Code	Package Description
1	NDC:71066-0001-1	10 mL in 1 VIAL

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/10/2016

Labeler - PROTOX Inc. (689846300)

Registrant - PROTOX Inc. (689846300)

Establishment
Name	Address	ID/FEI	Operations
PROTOX Inc.		689846300	manufacture(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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