Dermatop Topical Ointment 0.1pct Drug Medication Dosage Information
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Dermatop: Topical ointment (0.1%)

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What is this Medicine?

PREDNICARBATE (PRED ni kar bate) is a corticosteroid. It is used to treat skin problems that may cause itching, redness, and swelling.

In-Depth Information
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Dermatop 0.1% Topical Ointment

NDC: 000660508
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Contact Dermatitis, Keloids, Alopecia, Rhus Dermatitis, Necrobiosis Lipoidica Diabeticorum, Pompholyx, Eczema, Pemphigus, Sarcoidosis, Discoid Lupus Erythematosus, Granuloma Annulare, Seborrheic Dermatitis, Prurigo, Polymorphous Light Eruption, Pruritus, Pityriasis Rosea, Psoriasis, Lichen Striatus, Lichen Simplex, Atopic Dermatitis, Lichen Planus, Xerosis, Exfoliative Dermatitis

Storage Information
Store at room temperature (between 59 to 86 degrees F)
Dermatop 0.1% Topical Ointment

Reported Side Effects for Dermatop 0.1% Topical Ointment

Rash With Pustules Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Itching Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Dry Skin Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Skin Irritation Incidence:
1.0-10.0%*
Severity: MILD
Onset: EARLY
Skin Redness Incidence:
1.0-10.0%*
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

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


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