Label: ANUCORT-HC- hydrocortisone acetate suppository
- NDC Code(s): 0713-0503-01, 0713-0503-12, 0713-0503-24
- Packager: Cosette Pharmaceuticals, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 22, 2023
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- DESCRIPTION
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CLINICAL PHARMACOLOGY
In normal subjects, about 26% of hydrocortisone acetate is absorbed when the 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.
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
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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. - INFORMATION FOR PATIENTS
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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 to 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. -
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 SUSPECTED ADVERSE REACTIONS, contact Cosette Pharmaceuticals, Inc. at 1-800-922-1038 or FDA at 1-800-FDA-1088 orwww.fda.gov/medwatch. - DRUG ABUSE AND DEPENDENCE
- OVERDOSAGE
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DOSAGE AND ADMINISTRATION
For rectal administration. Detach one suppository from strip of suppositories. Hold suppository upright. Separate tabs at top opening and pull downward from the pointed end. Continue pulling downward to almost the full length of the suppository. Carefully remove the suppository from the pocket. Avoid excessive handling of the suppository which is designed to melt at body temperature. Insert suppository into the rectum with gentle pressure, 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
- STORAGE AND HANDLING
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PRINCIPAL DISPLAY PANEL
NDC 0713-0503-12
ANUCORT-HC TM
Hydrocortisone Acetate Suppositories
25 mg
Rx only
For Rectal Administration
12 Adult Suppositories
Cosette Pharmaceuticals, Inc.
NDC 0713-0503-24
ANUCORT-HC TM
Hydrocortisone Acetate Suppositories
25 mg
Rx only
For Rectal Administration
24 Adult Suppositories
Cosette Pharmaceuticals, Inc.
NDC 0713-0503-01
ANUCORT-HC TM
Hydrocortisone Acetate Suppositories
25 mg
Rx only
For Rectal Administration
100 Adult Suppositories
Cosette Pharmaceuticals, Inc.
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INGREDIENTS AND APPEARANCE
ANUCORT-HC
hydrocortisone acetate suppositoryProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0713-0503 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 25 mg Inactive Ingredients Ingredient Name Strength HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0713-0503-12 12 in 1 CARTON; Type 0: Not a Combination Product 01/15/1990 2 NDC:0713-0503-24 24 in 1 CARTON; Type 0: Not a Combination Product 01/15/1990 3 NDC:0713-0503-01 100 in 1 CARTON; Type 0: Not a Combination Product 01/15/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/15/1990 Labeler - Cosette Pharmaceuticals, Inc. (116918230) Registrant - Cosette Pharmaceuticals, Inc. (116918230) Establishment Name Address ID/FEI Business Operations Cosette Pharmaceuticals NC Laboratories, LLC 079419931 analysis(0713-0503) , label(0713-0503) , manufacture(0713-0503) , pack(0713-0503)
