Ciprofloxacin Otic Drops, Solution 0.2pct Drug Medication Dosage Information
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Ciprofloxacin: Otic drops, solution (0.2%)

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Ciprofloxacin 0.2% Otic Soln

What is this Medicine?

CIPROFLOXACIN (sip roe FLOX a sin) is used to treat ear infections.

Similar Brand Name Drugs : Cetraxal: Otic drops, solution (0.2%)
CVS Pharmacy Patient Statistics for Ciprofloxacin: Otic drops, solution(0.2%)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information

Ciprofloxacin 0.2% Otic Solution

NDC: 421950550
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Otitis Externa

Storage Information
Protect from light
Discard unused portion. Do not store for later use.
Store between 59 to 77 degrees F
Ciprofloxacin 0.2% Otic Solution

Reported Side Effects for Ciprofloxacin 0.2% Otic Solution

Vesicular Rash Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Lyell'S Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Darkened Skin Patches Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Bruises Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Rash With Pustules Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Flushing Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Rash Of Red Skin Bumps Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Skin Redness Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Diaphoresis Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Chills Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Blistery Rash Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Anaphylactoid Reactions Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Hives Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Stevens-Johnson Syndrome Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Itching Incidence:
<3.0%*
Severity: MILD
Onset: RAPID
Headache Incidence:
<3.9%*
Severity: MILD
Onset: EARLY
Fever Incidence:
<2.1%*
Severity: MILD
Onset: EARLY
Exfoliative Dermatitis Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Erythema Multiforme Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Angioedema Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Severe Allergy Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Skin Rash Incidence:
1.0-1.8%*
Severity: MILD
Onset: EARLY
Superinfection Incidence:
1.8-3.0%*
Severity: MODERATE
Onset: DELAYED
*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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