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Registry Hub
Peer-Reviewed Evidence
HomeDrug RegistryCompareALA CORT vs ACLOVATE
Comparative Pharmacology

ALA CORT vs ACLOVATE Comparison

Head-to-head clinical analysis & difference comparison: details on mechanism of action, dosing, half-life, interactions, and maternal-fetal safety.

Clinical EssentialsPharmacokineticsSpecial PopulationsSafety & MonitoringPregnancy & LactationClinical Insights
Differential Analysis

ALA-CORT vs ACLOVATE

Clinician-reviewed, head-to-head comparison of mechanism, dosing, pharmacokinetics, and safety profiles.

View ALA-CORT Monograph View ACLOVATE Monograph
ALA-CORT
Topical Corticosteroid
Category C
ACLOVATE
Topical Corticosteroid
Category C
TL;DR — Key Differences
  • Half-life: ALA-CORT has a half-life of Terminal elimination half-life: 1–2 hours for hydrocortisone (active component), prolonged in liver disease or with concurrent CYP3A4 inhibitors.; ACLOVATE has Terminal elimination half-life: approximately 6-8 hours after topical application; systemic absorption is minimal under normal use..
  • No direct drug-drug interaction has been documented between ALA-CORT and ACLOVATE.
  • Pregnancy: ALA-CORT is rated Category C; ACLOVATE is rated Category C.

Last clinically reviewed: July 2026 · OpiCalc Medical Review Team

Clinical Essentials

ALA-CORT
ACLOVATE
Mechanism of Action
ALA-CORT

Topical corticosteroid that induces phospholipase A2 inhibitory proteins, collectively called lipocortins, which inhibit the release of arachidonic acid, thereby reducing prostaglandin and leukotriene synthesis, and exerting anti-inflammatory, antipruritic, and vasoconstrictive effects.

ACLOVATE

Aclovate (alclometasone dipropionate) is a synthetic corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties. Its mechanism involves binding to glucocorticoid receptors, modulating gene expression to inhibit phospholipase A2, reducing arachidonic acid release, and decreasing prostaglandin and leukotriene synthesis.

Indications
ALA-CORT

Relief of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses (FDA),Off-label: Atopic dermatitis, psoriasis, contact dermatitis, lichen planus, discoid lupus erythematosus

ACLOVATE

Relief of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses (e.g., atopic dermatitis, contact dermatitis, eczema, psoriasis) - FDA approved,Off-label: Treatment of mild to moderate plaque psoriasis, seborrheic dermatitis, and lichen planus

Standard Dosing
ALA-CORT

Topical: Apply a thin film to affected area 3-4 times daily. Dosage strength: 0.5% cream or ointment.

ACLOVATE

Apply a thin film to affected skin areas twice daily. Not for ophthalmic, oral, or intravaginal use.

Direct Interaction
ALA-CORT
No Direct Interaction
ACLOVATE
No Direct Interaction

Pharmacokinetics

ALA-CORT
ACLOVATE
Half-Life
ALA-CORT

Terminal elimination half-life: 1–2 hours for hydrocortisone (active component), prolonged in liver disease or with concurrent CYP3A4 inhibitors.

ACLOVATE

Terminal elimination half-life: approximately 6-8 hours after topical application; systemic absorption is minimal under normal use.

Metabolism
ALA-CORT

Topically applied; systemic absorption is minimal but can be increased with use on large areas, occlusive dressings, or damaged skin. Absorbed portion is metabolized primarily in the liver via hepatic microsomal enzymes (CYP3A4) and excreted by the kidneys.

ACLOVATE

Aclovate is metabolized in the skin and liver via ester hydrolysis to inactive metabolites. Systemic metabolism primarily involves cytochrome P450 enzymes (CYP3A4) for any absorbed fraction, but extensive first-pass metabolism limits systemic exposure.

Excretion
ALA-CORT

Primarily hepatic metabolism (approximately 95%) followed by renal excretion of inactive metabolites (<5% unchanged). Biliary/fecal excretion is negligible.

ACLOVATE

Renal (primarily as metabolites, <5% unchanged), biliary/fecal (minor).

Protein Binding
ALA-CORT

Hydrocortisone is approximately 90–95% bound to corticosteroid-binding globulin (CBG, transcortin) and albumin.

ACLOVATE

Approximately 90%, primarily to albumin and corticosteroid-binding globulin (CBG).

VD (L/kg)
ALA-CORT

Apparent volume of distribution (Vd) is approximately 0.4–0.6 L/kg, indicating moderate tissue distribution and limited penetration into CNS.

ACLOVATE

Not well-characterized in topical use; after systemic absorption, Vd is approximately 1-2 L/kg, indicating distribution into tissues.

Bioavailability
ALA-CORT

Topical: Bioavailability is negligible (<1%) through intact skin; may increase (up to 30%) with damaged skin or occlusive dressings. Rectal: Bioavailability is approximately 10–20% via mucosal absorption, with first-pass metabolism reducing systemic exposure.

ACLOVATE

Topical: approximately 1-3% systemic absorption on intact skin; increased up to 15% on occluded or damaged skin.

Special Populations

ALA-CORT
ACLOVATE
Renal Adjustments
ALA-CORT

No adjustment required for topical use; systemic absorption minimal.

ACLOVATE

No dose adjustment required. Topical use with minimal systemic absorption.

Hepatic Adjustments
ALA-CORT

No adjustment required for topical use; hepatic metabolism negligible.

ACLOVATE

No dose adjustment required. Topical use with minimal systemic absorption.

Pediatric Dosing
ALA-CORT

Children ≥2 years: Apply a thin film to affected area 2-3 times daily. Use lowest potency preparation; avoid prolonged use.

ACLOVATE

Use smallest amount effective for shortest duration. Avoid prolonged use, occlusive dressings, or application to large surface areas. Safety in children <1 year not established.

Geriatric Dosing
ALA-CORT

Use lowest effective dose; monitor for skin atrophy and systemic effects due to thinner skin and increased percutaneous absorption.

ACLOVATE

Use with caution due to increased risk of skin atrophy and systemic absorption. Limit frequency and duration; avoid occlusive dressings.

Safety & Monitoring

ALA-CORT
ACLOVATE
Black Box Warnings
ALA-CORT
FDA Black Box Warning

None

ACLOVATE
FDA Black Box Warning

No FDA black box warning.

Warnings/Precautions
ALA-CORT

Systemic absorption may cause reversible HPA axis suppression,Cushing's syndrome, hyperglycemia, and glucosuria with prolonged use,Local adverse reactions: atrophy, striae, telangiectasias, acneiform eruptions, perioral dermatitis,May mask signs of infection,Use with caution in pediatric patients due to increased susceptibility to HPA axis suppression,Avoid use on face, intertriginous areas, and under occlusive dressings unless directed by physician

ACLOVATE

Topical corticosteroids can cause hypothalamic-pituitary-adrenal (HPA) axis suppression, especially with prolonged use, large surface area, occlusion, or in pediatric patients.,Reversible HPA axis suppression may occur after discontinuation.,Systemic effects including Cushing's syndrome, hyperglycemia, and glucosuria have been reported.,Local adverse reactions: burning, itching, irritation, dryness, folliculitis, hypopigmentation, allergic contact dermatitis, maceration, secondary infection, skin atrophy, striae, and miliaria.,Use caution in patients with impaired skin integrity or areas of skin atrophy.,Pediatric patients may be more susceptible to systemic toxicity due to higher skin surface-to-body-weight ratio.

Contraindications
ALA-CORT

Hypersensitivity to any component of the formulation,Untreated bacterial, viral, fungal, or parasitic skin infections,Viral skin infections (e.g., herpes simplex, varicella) at treatment site,Perioral dermatitis,Rosacea

ACLOVATE

Hypersensitivity to alclometasone dipropionate or any component of the formulation.,Untreated bacterial, fungal, or viral skin infections (e.g., herpes simplex, varicella, tuberculosis of the skin).

Adverse Reactions
ALA-CORT
Data Pending
ACLOVATE
Data Pending
Food Interactions
ALA-CORT

No known food interactions with topical ALA-CORT.

ACLOVATE

No known food interactions with topical Aclovate.

Pregnancy & Lactation

ALA-CORT
ACLOVATE
Teratogenic Risk
ALA-CORT

FDA Pregnancy Category C. First trimester: No adequate human studies; animal studies show increased risk of cleft palate. Second/third trimester: Risk of intrauterine growth restriction, adrenal suppression in fetus. Avoid prolonged use.

ACLOVATE

Topical corticosteroids like ACLOVATE (alclometasone dipropionate) are generally considered low risk in pregnancy, but systemic absorption can occur. Class C: Fetal risk cannot be ruled out. Avoid extensive use or prolonged treatment, especially in first trimester. Second and third trimester: Use only if clearly needed, minimal area and duration.

Lactation Summary
ALA-CORT

Provides small amounts in breast milk; M/P ratio unknown. At maternal doses up to 80 mg/day, no adverse effects reported in infants. Consider risk-benefit with high doses or prolonged therapy.

ACLOVATE

Safety unknown; likely minimal systemic absorption due to low potency. M/P ratio not established. Avoid application to breasts or large areas; use caution.

Pregnancy Dosing
ALA-CORT

Pregnancy-induced pharmacokinetic changes (increased clearance, volume of distribution) may require increased dosing, but clinical response should guide adjustment. Avoid high doses and prolonged use.

ACLOVATE

No standard dose adjustment required; however, limit potency, frequency, and duration to lowest effective due to altered skin permeability. No pharmacokinetic changes necessitate dose change.

Maternal Safety Status
ALA-CORT
Category C
ACLOVATE
Category C

Clinical Insights

ALA-CORT
ACLOVATE
Clinical Pearls
ALA-CORT

ALA-CORT (hydrocortisone acetate 2.5% and pramoxine HCl 1%) is a topical corticosteroid with anesthetic. Use for short-term relief of pruritus and inflammation in corticosteroid-responsive dermatoses. Avoid prolonged use on intertriginous or occluded areas. Limit to <2 weeks continuous use in adults to avoid skin atrophy. Not recommended for children <2 years.

ACLOVATE

Topical corticosteroids like Aclovate are classified as low-potency (Group VI). They are suitable for thin skin areas (e.g., face, flexures) and for children. Avoid prolonged use without interruption to minimize systemic absorption, especially in pediatric patients due to higher skin surface area-to-body weight ratio.

Patient Counseling
ALA-CORT

Apply a thin layer to affected area no more than 3-4 times daily.,Do not cover with bandages or plastic unless directed by doctor.,Avoid contact with eyes, mouth, or broken skin.,Discontinue and notify doctor if infection, irritation, or no improvement after 7 days.,Do not use for diaper dermatitis or under diapers/occlusive dressings.,Keep out of reach of children.

ACLOVATE

Apply a thin layer to affected skin only, not to normal surrounding skin.,Do not cover with bandages or dressings unless directed by your doctor.,Use for the prescribed duration; do not use longer than 2 weeks at a time.,Avoid contact with eyes, mouth, and open wounds.,Report any signs of skin thinning, redness, or irritation to your healthcare provider.

Safety Verification

Known Interactions

ALA-CORT Risks

No interactions on record

ACLOVATE Risks

No interactions on record

Compare Alternatives

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ACLOVATE vs ALPHADERMTopical Corticosteroid
ALA-CORT vs AMCINONIDETopical Corticosteroid
Clinical Q&A

Frequently Asked Questions

Common clinical questions about ALA-CORT vs ACLOVATE, answered by our medical review team.

1. What is the main difference between ALA-CORT and ACLOVATE?

ALA-CORT is a Topical Corticosteroid that works by Topical corticosteroid that induces phospholipase A2 inhibitory proteins, collectively called lipocortins, which inhibit the release of arachidonic acid, thereby reducing prostaglandin and leukotriene synthesis, and exerting anti-inflammatory, antipruritic, and vasoconstrictive effects.. ACLOVATE is a Topical Corticosteroid that works by Aclovate (alclometasone dipropionate) is a synthetic corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictive properties. Its mechanism involves binding to glucocorticoid receptors, modulating gene expression to inhibit phospholipase A2, reducing arachidonic acid release, and decreasing prostaglandin and leukotriene synthesis.. They differ in pharmacokinetic profiles, FDA-approved indications, and side effect profiles.

2. Which is stronger: ALA-CORT or ACLOVATE?

Potency comparisons between ALA-CORT and ACLOVATE depend on the specific clinical indication. These are both Topical Corticosteroid agents and are not directly interchangeable by dose. A physician or clinical pharmacist should guide any therapeutic switching decisions.

3. What is the standard dosing for ALA-CORT vs ACLOVATE?

The standard adult dose of ALA-CORT is: Topical: Apply a thin film to affected area 3-4 times daily. Dosage strength: 0.5% cream or ointment.. The standard adult dose of ACLOVATE is: Apply a thin film to affected skin areas twice daily. Not for ophthalmic, oral, or intravaginal use.. Dosing should always be individualized based on indication, renal and hepatic function, age, and other patient factors.

4. Can you take ALA-CORT and ACLOVATE together?

No direct drug-drug interaction has been formally documented between ALA-CORT and ACLOVATE in current clinical databases. However, individual patient risk factors including other medications, organ function, and comorbidities should always be evaluated by a qualified healthcare provider.

5. Are ALA-CORT and ACLOVATE safe during pregnancy?

The maternal-fetal safety profiles differ. ALA-CORT is classified as Category C. FDA Pregnancy Category C. First trimester: No adequate human studies; animal studies show increased risk of cleft palate. Second/third trimester: Risk of intrauterine growth restri. ACLOVATE is classified as Category C. Topical corticosteroids like ACLOVATE (alclometasone dipropionate) are generally considered low risk in pregnancy, but systemic absorption can occur. Class C: Fetal risk cannot be . Always consult a maternal-fetal medicine specialist before taking either drug during pregnancy or lactation.