Business Hours: Monday-Friday 9AM-6PM EST
Brand:
BOTOX®
Manufacturer:
Allergan
Active Substance(s):
BOTULINUM TOXIN TYPE A
Strength:
100u
Pack size:
1 x 100u Vial
BOTOX® is a botulinum type A product, a wrinkle injection that treats glabellar lines and other wrinkles by temporarily blocking the release of acetylcholine from nerves, helping prevent muscle movement in the area and relaxing the skin.
BOTOX Cosmetic is an acetylcholine release inhibitor and a neuromuscular blocking agent indicated in adult patients for the temporary improvement in the appearance of:
BOTOX is a muscle relaxant used to treat a number of conditions within the body. It contains the active substance botulinum toxin type A and is injected into either the muscles, the bladder wall, or deep into the skin. It works by partially blocking the nerve impulses to any muscles that have been injected and reduces excessive contractions of these muscles. BOTOX can be used to reduce sweat production, improve the appearance of lines between the eyebrows (glabellar lines), crow’s feet lines from the corner of the eyes, or forehead lines at maximum raised eyebrows. It may also be used to treat urinary incontinence and chronic migraine.
The potency Units of BOTOX Cosmetic (onabotulinumtoxinA) for injection are specific to the preparation and assay method utilized. They are not interchangeable with other preparations of botulinum toxin products. Indication-specific dosage and administration recommendations should be followed. In treating adult patients for one or more indications with BOTOX and BOTOX Cosmetic, the maximum cumulative dose should generally not exceed 400 Units in a 3-month interval. The safety and effectiveness of dosing with BOTOX Cosmetic more frequently than every 3 months have not been clinically evaluated. The safe and effective use of BOTOX Cosmetic depends upon proper storage of the product, selection of the correct dose, and proper reconstitution and administration techniques. Physicians administering BOTOX Cosmetic must understand the relevant neuromuscular and structural anatomy of the area involved and any alterations to the anatomy due to prior surgical procedures and disease.
BOTOX is contraindicated in patients with hypersensitivity to any botulinum toxin preparation or any of the components in the formulation, and in the case of infection at the injection site.
Patients receiving concomitant treatment of BOTOX Cosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (e.g., curare-like agents) or muscle relaxants should be observed closely because the effect of BOTOX Cosmetic may be potentiated.
BOTOX® is a botulinum type A product, a wrinkle injection that treats glabellar lines and other wrinkles by temporarily blocking the release of acetylcholine from nerves, helping prevent muscle movement in the area and relaxing the skin.
BOTOX Cosmetic is an acetylcholine release inhibitor and a neuromuscular blocking agent indicated in adult patients for the temporary improvement in the appearance of:
BOTOX is a muscle relaxant used to treat a number of conditions within the body. It contains the active substance botulinum toxin type A and is injected into either the muscles, the bladder wall, or deep into the skin. It works by partially blocking the nerve impulses to any muscles that have been injected and reduces excessive contractions of these muscles. BOTOX can be used to reduce sweat production, improve the appearance of lines between the eyebrows (glabellar lines), crow’s feet lines from the corner of the eyes, or forehead lines at maximum raised eyebrows. It may also be used to treat urinary incontinence and chronic migraine.
The potency Units of BOTOX Cosmetic (onabotulinumtoxinA) for injection are specific to the preparation and assay method utilized. They are not interchangeable with other preparations of botulinum toxin products. Indication-specific dosage and administration recommendations should be followed. In treating adult patients for one or more indications with BOTOX and BOTOX Cosmetic, the maximum cumulative dose should generally not exceed 400 Units in a 3-month interval. The safety and effectiveness of dosing with BOTOX Cosmetic more frequently than every 3 months have not been clinically evaluated. The safe and effective use of BOTOX Cosmetic depends upon proper storage of the product, selection of the correct dose, and proper reconstitution and administration techniques. Physicians administering BOTOX Cosmetic must understand the relevant neuromuscular and structural anatomy of the area involved and any alterations to the anatomy due to prior surgical procedures and disease.
BOTOX is contraindicated in patients with hypersensitivity to any botulinum toxin preparation or any of the components in the formulation, and in the case of infection at the injection site.
Patients receiving concomitant treatment of BOTOX Cosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (e.g., curare-like agents) or muscle relaxants should be observed closely because the effect of BOTOX Cosmetic may be potentiated.
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