MedPath

Hydrocortisone Acetate

Hydrocortisone Acetate Suppositories, 25 mgFor Rectal AdministrationRx only

Approved
Approval ID

b9efefd3-76a6-4450-b770-641c3585b3e6

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 19, 2021

Manufacturers
FDA

Cameron Pharmaceuticals, LLC

DUNS: 078371442

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

HYDROCORTISONE ACETATE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code42494-301
Product Classification
G
Generic Name
HYDROCORTISONE ACETATE
Product Specifications
Route of AdministrationRECTAL
Effective DateOctober 19, 2021
FDA Product Classification

INGREDIENTS (2)

HYDROCORTISONE ACETATEActive
Quantity: 25 mg in 1 1
Code: 3X7931PO74
Classification: ACTIB
C10-18 TRIGLYCERIDESInactive
Code: 43AGM4PHPI
Classification: IACT

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 10/19/2021

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

NDC 42494-301-12

Hydrocortisone Acetate Suppositories

25 mg

FOR RECTAL USE ONLY

12 Suppositories
Unit Dose

Rx Only

AnusolCarton.jpg

INDICATIONS & USAGE SECTION

LOINC: 34067-9Updated: 10/19/2021

INDICATIONS AND USAGE:

Hydrocortisone acetate suppositories are indicated for use in inflamed hemorrhoids, post-irradiation (factitial) proctitis, as an adjunct in the treatment of chronic ulcerative colitis, cryptitis, other inflammatory conditions of anorectum, and pruritus ani.

CONTRAINDICATIONS SECTION

LOINC: 34070-3Updated: 10/19/2021

CONTRAINDICATIONS:

Hydrocortisone acetate suppositories are contraindicated in those patients having a history of hypersensitivity to hydrocortisone acetate or any of the components.

ADVERSE REACTIONS SECTION

LOINC: 34084-4Updated: 10/19/2021

ADVERSE REACTIONS:

The following local adverse reactions have been reported with hydrocortisone acetate suppositories; burning, itching, irritation, dryness, folliculitis, hypopigmentation, allergic contact dermatitis, secondary infection.

To report an adverse event, please contact Cameron Pharmaceuticals, LLC at 1-888-767-7913.

DESCRIPTION SECTION

LOINC: 34089-3Updated: 10/19/2021

DESCRIPTION

Hydrocortisone acetate is a corticosteroid designed chemically as pregn-4-ene-3, 20-dione, 21-(acetyloxy)-11, 17-dihydroxy-(11ß) with the following structural formula:

![Structural Formula](/dailymed/image.cfm?name=anusol- hc_7335-figure-1-2-17-2011_2-31-54_PM.jpg&id=591793)

Each suppository for rectal administration contains hydrocortisone acetate, USP 25 mg in a specially blended hydrogenated vegetable base.

CLINICAL PHARMACOLOGY SECTION

LOINC: 34090-1Updated: 10/19/2021

CLINICAL PHARMACOLOGY:

In normal subjects, about 26% of hydrocortisone acetate is absorbed when the hydrocortisone acetate suppository is applied to the rectum. Absorption of hydrocortisone acetate may vary across abraded or inflamed surfaces.

Topical steroids are primarily effective because of their anti-inflammatory, anti-pruritic and vasoconstrictive action.

PRECAUTIONS SECTION

LOINC: 42232-9Updated: 10/19/2021

PRECAUTIONS:

Do not use hydrocortisone acetate suppositories unless adequate proctologic examination is made.

If irritation develops, the product should be discontinued and appropriate therapy instituted.

In the presence of an infection, the use of an appropriate antifungal or antibacterial agent should be instituted. If a favorable response does not occur promptly, hydrocortisone acetate should be discontinued until the infection has been adequately controlled.

Carcinogenesis:

No long-term studies in animals have been performed to evaluate the carcinogenic potential of corticosteroid suppositories.

PREGNANCY SECTION

LOINC: 42228-7Updated: 10/19/2021

Pregnancy Category C:

In laboratory animals, topical steroids have been associated with an increase in the incidence of fetal abnormalities when gestating females have been exposed to rather low dosage levels. There are no adequate and well-controlled studies in pregnant women.

Hydrocortisone acetate suppositories should only be used during pregnancy if the potential benefit justifies the risk of the fetus. Drugs of this class should not be used extensively on pregnant patients, in large amounts, or for prolonged periods of time.

It is not known whether this drug is excreted in human milk, and because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from hydrocortisone acetate suppositories, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

DRUG ABUSE AND DEPENDENCE SECTION

LOINC: 42227-9Updated: 10/19/2021

DRUG ABUSE AND DEPENDENCE:

Drug abuse and dependence have not been reported in patients treated with hydrocortisone acetate suppositories.

OVERDOSAGE SECTION

LOINC: 34088-5Updated: 10/19/2021

OVERDOSAGE:

If signs and symptoms of systemic overdosage occur, discontinue use.

DOSAGE & ADMINISTRATION SECTION

LOINC: 34068-7Updated: 10/19/2021

DOSAGE AND ADMINISTRATION:

FOR RECTAL ADMINISTRATION. Detach one suppository from strip of suppositories. Hold suppository upright and carefully separate tabs at top opening and pull downward from the pointed end to expose the suppository. Remove the suppository from the pocket. Avoid excessive handling of suppository which is designed to melt at body temperature. Insert one suppository rectally, pointed end first. Insert one suppository in the rectum twice daily, morning and night for two weeks, in nonspecific proctitis. In more severe cases, one suppository three times a day or two suppositories twice daily. In factitial proctitis, the recommended duration of therapy is six to eight weeks or less, according to the response of the individual case.

HOW SUPPLIED SECTION

LOINC: 34069-5Updated: 10/19/2021

HOW SUPPLIED:

Hydrocortisone acetate suppositories 25mg are off-white, smooth surfaced and bullet shaped with one pointed end.

Box of 12 suppositories, NDC 42494-301-12

Box of 24 suppositories, NDC 42494-301-24

STORAGE AND HANDLING SECTION

LOINC: 44425-7Updated: 10/19/2021

STORAGE:

Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature]. Excursions permitted to 15°-30°C (59°-86°F). Store away from heat. Protect from freezing. Avoid contact with eyes.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

SPL UNCLASSIFIED SECTION

LOINC: 42229-5Updated: 10/19/2021

PHARMACIST:

This product is not an Orange Book rated product, therefore all prescriptions using this product shall be subject to state and federal statutes as applicable. This product has not been subjected to FDA therapeutic or other equivalency testing. There are no claims of bioequivalence or therapeutic equivalence. Each person recommending a prescription substitution using this product shall make such recommendation based on his/her professional knowledge and opinion, upon evaluating the active ingredients, inactive ingredients, excipients and chemical information contained within the enclosed prescribing information.

Rx Only

Manufactured for:
Cameron Pharmaceuticals, LLC
Louisville, KY 40245

Rev. 07/16

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