Carmol Hc Topical Cream 1-10pct Drug Medication Dosage Information
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Carmol HC: Topical cream (1-10%)

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What is this Medicine?

HYDROCORTISONE; UREA (hye droe KOR ti sone; yoo REE uh) is a combination of a corticosteroid and a moisturizer. It is used on the skin to reduce swelling, redness, itching, and skin irritation.

In-Depth Information

Carmol HC 1%-10% Topical Cream

NDC: 103370550
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Pruritus, Skin Inflammation, Psoriasis, Atopic Dermatitis, Xerosis

Storage Information
Store at room temperature (between 59 to 86 degrees F)
Protect from freezing
Carmol HC 1%-10% Topical Cream

Reported Side Effects for Carmol HC 1%-10% Topical Cream

Striae Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Growth Inhibition Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Glycosuria Incidence:
<1.0%*
Severity: MODERATE
Onset: EARLY
Infection Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Hypothalamic-pituitary-adrenal (HPA) Suppression Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Increased Blood Sugar Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Dry Skin Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
Unusual Skin Lightening Incidence:
<1.0%*
Severity: MILD
Onset: DELAYED
High Pressure In Brain Incidence:
<1.0%*
Severity: SEVERE
Onset: EARLY
Cushing's Syndrome Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Low Steroid Hormones Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Itching Incidence:
1.0-10.0%*
Severity: MILD
Onset: RAPID
Inflamed Hair Follicles Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Thinning Of Skin Incidence:
1.0-10.0%*
Severity: SEVERE
Onset: DELAYED
Drug-Induced Acne Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Allergic Skin Reaction Incidence:
1.0-10.0%*
Severity: MODERATE
Onset: DELAYED
Ambras Syndrome Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Sweat Rash Incidence:
1.0-10.0%*
Severity: MILD
Onset: DELAYED
Skin Irritation Incidence:
1.0-10.0%*
Severity: MILD
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.


Learning More About
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