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Description
VANIQA (pronounced "VAN-i-ka") is a prescription medication applied to the skin for the reduction of unwanted facial hair in women. The active ingredient in VANIQA is eflornithine hydrochloride. VANIQ
A also contains ceteareth-20, cetearyl alcohol, dimethicone, glyceryl stearate, methylparaben, mineral oil, PEG-100 stearate, phenoxyethanol, propylparaben, stearyl alcohol and water.
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Before Using This Medicine
Other medicines¡XAlthough certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your do
or may want to change the dose, or other precautions may be necessary. Tell your health care professional if you are using any other topical prescription or nonprescription (over-the-counter [OTC]) me
dicine that is to be applied to the same area of the skin.
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Precautions while Using this Medicine
If skin irritation occurs, reduce the frequency of treatments. If irritation continues, stop using the medicine and contact your doctor.
If no improvement is seen after six months of treatme
nt, stop using the medicine and contact your doctor.
If condition gets worse while you use the medicine, stop the medicine and contact your doctor.
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Other Medicines
Vaniqa has no known drug interactions. Make sure your doctor is aware of all medications and facial products you are using before you begin Vaniqa treatments.
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Possible Side Effect
Vaniqa is intended for any woman who has unwanted facial hair around their lips or under their chin. If you are allergic to any of the active ingredients, let your doctor know. Vaniqa contains ingredi
ents including Vaniqa also contains ceteareth-20, cetearyl alcohol, dimethicone, glyceryl stearate, methylparaben, mineral oil, PEG-bO stearate, phenoxyethanol, propylparaben, stearyl alcohol and wate
r
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How should you take this medication?
Overdosage information with VANIQA is unavailable. Given the low percutaneous penetration of this drug, overdosage via the topical route is not expected (see CLINICAL PHARMACOLOGY ). However, should v
ery high topical doses (e.g., multiple tubes per day) or oral ingestion be encountered (a 30 g tube contains 4.2 g of eflornithine hydrochloride), the patient should be monitored, and appropriate supp
ortive measures administered as necessary.
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