ALACORT- hydrocortisone cream
Alacort by
Drug Labeling and Warnings
Alacort by is a Prescription medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- For external use only
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DESCRIPTION
The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents. Hydrocortisone is a member of this class. Chemically hydrocortisone is pregn-4-ene-3, 20-dione, 11, 17, 21-trihydroxy-, (11β)-. Its molecular formula is C 21H 30O 5 and molecular weight is 362.47. Its structural formula is:
Each gram of ALA-CORT ® (Hydrocortisone Cream USP) 1% contains 10 mg hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
Each gram of ALA-CORT® (Hydrocortisone Cream USP) 2.5% contains 25 mg hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
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CLINICAL PHARMACOLOGY
Topical corticosteroids share anti-inflammatory, antipruritic and vasoconstrictive actions.
The mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. Various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. There is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man.
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Pharmacokinetics
The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings.
Topical corticosteroids can be absorbed from normal intact skin. Inflammation and/or other disease processes in the skin increase percutaneous absorption. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. Thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses. (See DOSAGE AND ADMINISTRATION).
Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Corticosteroids are bound to plasma proteins in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
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Precautions
General
Systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing’s syndrome, hyperglycemia, and glucosuria in some patients.
Conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings.
Therefore, patients receiving a large dose of a potent topical steroid applied to a large surface area or under an occlusive dressing should be evaluated periodically for evidence of HPA axis suppression by using the urinary free cortisol and ACTH stimulation tests. If HPA axis suppression is noted, an attempt should be made to withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid.
Recovery of HPA axis function is generally prompt and complete upon discontinuation of the drug. Infrequently, signs and symptoms of steroid withdrawal may occur, requiring supplemental systemic corticosteroids.
Children may absorb proportionally larger amounts of topical corticosteroids and thus be more susceptible to systemic toxicity (See PRECAUTIONS-Pediatric Use).
If irritation develops, topical corticosteroids should be discontinued and appropriate therapy instituted.
In the presence of dermatological infections, the use of an appropriate antifungal or antibacterial agent should be instituted. If a favorable response does not occur promptly, the corticosteroid should be discontinued until the infection has been adequately controlled.
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Information for the Patient
Patients using topical corticosteroids should receive the following information and instructions:
1. This medication is to be used as directed by the physician. It is for external use only. Avoid contact with the eyes.
2. Patients should be advised not to use this medication for any disorder other than for which it was prescribed.
3. The treated skin area should not be bandaged or otherwise covered or wrapped as to be occlusive unless directed by the physician.
4. Patients should report any signs of local adverse reactions especially under occlusive dressing.
5. Parents of pediatric patients should be advised not to use tight-fitting diapers or plastic pants on a child being treated in the diaper area, as these garments may constitute occlusive dressings.
- Latoratory Tests
- Carcinogenesis, Mutagenesis, and Impairment of Fertility
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Pregnancy: Teratogenic effects - Pregnancy Category C
Corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. The more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. There are no adequate and well-controlled studies in pregnant women on teratogenic effects from topically applied corticosteroids. Therefore, topical corticosteroids should be used during pregnancy only if the potential benefit justifies the potential 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.
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Nursing Mothers
It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in breast milk. Systemically administered corticosteroids are secreted into breast milk in quantities not likely to have a deleterious effect on the infant. Nevertheless, caution should be exercised when topical corticosteroids are administered to a nursing woman.
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Pediatric Use
Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced HPA axis suppression and Cushing’s syndrome than mature patients because of a larger skin surface area to body weight ratio.
Hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing’s syndrome, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. Manifestations of adrenal suppression in pediatric patients include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to ACTH stimulation. Manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema.
Administration of topical corticosteroids to pediatric patients should be limited to the least amount compatible with an effective therapeutic regimen. Chronic corticosteroid therapy may interfere with the growth and development of pediatric patients.
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ADVERSE REACTIONS
The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, foliculitiis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria.
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OVERDOSAGE
Topically applied corticosteroids can be absorbed in sufficient amounts to produce systems effects (See PRECAUTIONS).
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DOSAGE AND ADMINISTRATION
Topical corticosteroids are generally applied to the affected area as a thin film from two to four times daily depending on the severity of the condition.
Occlusive dressings may be used for the management of psoriasis or recalcitrant conditions. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.
- PACKAGING AND STORAGE
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HOW SUPPLIED
ALA-CORT ® (Hydrocortisone Cream USP), 1% is supplied in:
1 ounce (28.4 grams) tube NDC: 0316-0126-01
3 ounce (85.2 grams) tube NDC: 0316-0126-03
ALA-CORT® (Hydrocortisone Cream USP), 2.5% is supplied in:
20 grams tube NDC: 0316-0128-20
30 grams tube NDC: 0316-0128-30
454 grams jar NDC: 0316-0128-16
Manufactured and Distributed by: Crown Laboratories, Inc., Johnson City, Tennessee 37604
PRINTED IN USA
Revised: OCT 2015
P8000.03
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ALA-CORT (Hydrocortisone Cream USP), 1% - 1oz Label
NDC: 0316-0126-01
Rx Only
ALA-CORT ®
Hydrocortisone Cream USP, 1%
Warning: Keep out of reach of children.
For external use only.
Not for ophthalmic use.
1oz (28.4 grams)
Each gram contains: 10 mg Hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
Usual Dosage: 2 to 4 applications daily. See package insert for full prescribing information.
TO OPEN: Use cap to pucture seal. IMPORTANT: Do not use if seal has been puctured or is not visible.
Store at 20 o-25 oC (68 o-77 oF)[see USP Controlled Room Temperature].
See crimp of tube for Lot Number and Expiration Date.
Manufactured and Distributed by:
Crown Laboratories, Inc.
Johnson City, TN 37604
P2006.00
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ALA-CORT (Hydrocortisone Cream USP), 1% -1oz Carton
NDC: 0316-0126-01
Rx Only
ALA-CORT ®
Hydrocortisone Cream USP, 1%
Warning: Keep out of reach of children.
For external use only.
Not for ophthalmic use.
1oz (28.4 grams)
Each gram contains: 10 mg Hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
Directions for puncturing tube seal: Remove cap. Turn cap upside down and place puncture tip onto tube. Push cap until tube end is punctured. Screw cap back on to reseal tube.
Store at 20 o-25 oC (68 o-77 oF)[see USP Controlled Room Temperature].
Usual Dosage: 2 to 4 applications daily. See package insert for full prescribing information.
See end of carton for Lot Number and Expiration Date.Manufactured and Distributed by:
Crown Laboratories, Inc. Johnson City, TN 37604
P7003.02
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ALA-CORT (Hydrocortisone Cream USP), 2.5% - 30 grams tube
NDC: 0316-0128-30
Rx Only
ALA-CORT ®
Hydrocortisone Cream USP, 2.5%
Warning: Keep out of reach of children.
For external use only.
Not for ophthalmic use.
30 grams
Each gram contains: 25 mg Hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
Usual Dosage: 2 to 4 applications daily. See package insert for full prescribing information.
TO OPEN: Use cap to pucture seal. IMPORTANT: Do not use if seal has been puctured or is not visible.
Store at 20 o-25 oC (68 o-77 oF)[see USP Controlled Room Temperature].
See crimp of tube for Lot Number and Expiration Date.
Manufactured and Distributed by:
Crown Laboratories, Inc.
Johnson City, TN 37604
P2002.00
-
ALA-CORT (Hydrocortisone Cream USP), 2.5% - 30 grams carton
NDC: 0316-0128-30
Rx Only
ALA-CORT ®
Hydrocortisone Cream USP, 2.5%
Warning: Keep out of reach of children.
For external use only.
Not for ophthalmic use.
30 grams
Each gram contains: 25 mg Hydrocortisone USP in a cream base consisting of purified water, cetyl alcohol, glycerin, stearyl alcohol, propylene glycol, sodium lauryl sulfate, cetyl palmitate and sorbic acid.
Directions for puncturing tube seal: Remove cap. Turn cap upside down and place puncture tip onto tube. Push cap until tube end is punctured. Screw cap back on to reseal tube.
Store at 20 o-25 oC (68 o-77 oF)[see USP Controlled Room Temperature].
Usual Dosage: 2 to 4 applications daily. See package insert for full prescribing information.
See end of carton for Lot Number and Expiration Date.
Manufactured and Distributed by:
Crown Laboratories, Inc. Johnson City, TN 37604
P2003.00
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INGREDIENTS AND APPEARANCE
ALACORT
hydrocortisone creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 0316-0126 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) CETYL PALMITATE (UNII: 5ZA2S6B08X) SORBIC ACID (UNII: X045WJ989B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 0316-0126-01 1 in 1 CARTON 03/09/1973 1 28.4 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC: 0316-0126-03 1 in 1 CARTON 03/09/1973 2 85.2 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA080706 03/09/1973 ALACORT
hydrocortisone creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 0316-0128 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE 25 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM LAURYL SULFATE (UNII: 368GB5141J) CETYL PALMITATE (UNII: 5ZA2S6B08X) SORBIC ACID (UNII: X045WJ989B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 0316-0128-20 1 in 1 CARTON 01/06/2016 1 20 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC: 0316-0128-30 1 in 1 CARTON 01/06/2016 2 30 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC: 0316-0128-16 454 g in 1 JAR; Type 0: Not a Combination Product 01/06/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA080706 01/06/2016 Labeler - Crown Laboratories (079035945) Registrant - Crown Laboratories (079035945) Establishment Name Address ID/FEI Business Operations Crown Laboratories 079035945 manufacture(0316-0126, 0316-0128)
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