Botox Powder For Solution For Injection 100U Drug Medication Dosage Information
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Botox: Powder for solution for injection (100U)

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Botox 100unit Pwd for Inj

What is this Medicine?

ONABOTULINUMTOXINA (o na BOTT you lye num tox in eh) is a neuro-muscular blocker. This medicine is used to treat crossed eyes, eyelid spasms, severe neck muscle spasms, and elbow, wrist, and finger muscle spasms. It is also used to treat excessive underarm sweating, to prevent chronic migraine headaches, and to treat loss of bladder control due to neurologic conditions such as multiple sclerosis or spinal cord injury.

CVS Pharmacy Patient Statistics for Botox: Powder for solution for injection(100U)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Botox 100unit Powder for Injection

NDC: 000231145
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Cervical Dystonia, Hyperhidrosis, Blepharospasm, Migraine Prophylaxis, Neurogenic Bladder, Urinary Incontinence, Overactive Bladder (OAB), Spasticity, Strabismus

Sometimes used for but not FDA approved for the following conditions:
Achalasia, Sialorrhea, Neurogenic Bladder

Storage Information
Store unreconstituted product in refrigerator (36 to 46 degrees F)
Store reconstituted product in refrigerator (36 to 46 degrees F) and administer within 24 hours
Discard product if it contains particulate matter, is cloudy, or discolored
Store product in refrigerator (36 to 46 degrees F) for up to 36 months from date of manufacture
Botox 100unit Powder for Injection

Reported Side Effects for Botox 100unit Powder for Injection

Swollen Eyelids Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
<10.0%*
Severity: MILD
Onset: EARLY
Hypertropia Incidence:
<17.0%*
Severity: MODERATE
Onset: EARLY
Drooping Eyelids Incidence:
<21.0%*
Severity: MILD
Onset: DELAYED
Paresis Incidence:
<2.0%*
Severity: MODERATE
Onset: DELAYED
Bleeding Within The Eye Incidence:
<0.3%*
Severity: SEVERE
Onset: DELAYED
Muscle Weakness Incidence:
<4.0%*
Severity: MODERATE
Onset: DELAYED
Muscle And/Or Bone Pain Incidence:
<4.0%*
Severity: MILD
Onset: EARLY
Crossed Eyes Incidence:
<17.0%*
Severity: MODERATE
Onset: EARLY
Muscle Pain Incidence:
<3.0%*
Severity: MILD
Onset: EARLY
Eye Inflammatoin Incidence:
<6.0%*
Severity: SEVERE
Onset: DELAYED
Inability To Sleep Incidence:
<2.0%*
Severity: MILD
Onset: EARLY
High Blood Pressure Incidence:
<2.0%*
Severity: MODERATE
Onset: EARLY
Excessive Sweating Incidence:
<10.0%*
Severity: MILD
Onset: DELAYED
Headache Incidence:
<5.0%*
Severity: MILD
Onset: EARLY
Shortness Of Breath Incidence:
<4.5%*
Severity: MODERATE
Onset: EARLY
Drowsiness Incidence:
<10.0%*
Severity: MILD
Onset: EARLY
Nervousness Incidence:
<10.0%*
Severity: MILD
Onset: DELAYED
Infection Incidence:
<12.0%*
Severity: MILD
Onset: DELAYED
Blood In The Urine Incidence:
<4.0%*
Severity: MODERATE
Onset: DELAYED
Difficulty Swallowing Incidence:
<19.0%*
Severity: MODERATE
Onset: DELAYED
Dry Eyes Incidence:
<6.0%*
Severity: MILD
Onset: EARLY
Balance Problems Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Retaining Urine Incidence:
<17.0%*
Severity: MODERATE
Onset: EARLY
Itching Incidence:
<10.0%*
Severity: MILD
Onset: RAPID
Back Pain Incidence:
2.0-10.0%*
Severity: MILD
Onset: DELAYED
Weakness Incidence:
2.0-10.0%*
Severity: MILD
Onset: DELAYED
Dysarthria Incidence:
2.0-10.0%*
Severity: MODERATE
Onset: DELAYED
Dry Mouth Incidence:
2.0-10.0%*
Severity: MILD
Onset: EARLY
Injection Site Reaction Incidence:
2.0-10.0%*
Severity: MILD
Onset: RAPID
Bruise Incidence:
2.0-10.0%*
Severity: MILD
Onset: DELAYED
Upset Stomach Incidence:
2.0-10.0%*
Severity: MILD
Onset: EARLY
Painful Urination Incidence:
4.0-9.0%*
Severity: MODERATE
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Compatible - This drug is generally safe to take by nursing mothers.


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