Otc - Active Ingredient
Clostridium botulinum Toxin Type A
Protoxin
FDA Label NDC 71066-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Protox Inc. for the product Protoxin (NDC 71066-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, warnings, dosage & administration, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Normal human serum albumin, Sodium chloride
Otc - Purpose
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.
Warnings
Confirm the validity of the product label
to make sure the sterilizatios is not damaged before using
Dosage & Administration
N/A
Indications & Usage
N/A
Package Label.Principal Display Panel
Product Label (Label)
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