Utopic Topical Cream 41pct Drug Medication Dosage Information
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Utopic: Topical cream (41%)

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In-Depth Information

Utopic 41% Topical Cream

NDC: 578930301
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)




FDA approved for the following conditions:
Ichthyosis, Onychomycosis, Xerosis

Storage Information
Do not expose product to temperatures above 77 degrees F
Store between 59 to 77 degrees F, excursions permitted to 59 to 86 degrees F
Protect from freezing
Avoid excessive heat (above 104 degrees F)
Utopic 41% Topical Cream
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

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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