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.
Dermatop 0.1% Topical Ointment
NDC: 001875183-
Prescription Required
-
Not a Controlled Drug
(CSA Schedule) -
FDA Approved
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
Store at room temperature (between 59 to 86 degrees F)
Reported Side Effects for Dermatop 0.1% Topical Ointment
Onset: EARLY
Onset: RAPID
Onset: DELAYED
Onset: EARLY
Onset: EARLY
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.
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.
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.
Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.
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