Skip to content

Calcipotriene

Published: July 26, 2026Updated: July 26, 2026

Calcipotriene is a synthetic vitamin D3 analogue used primarily to treat plaque psoriasis. When combined with betamethasone dipropionate (a corticosteroid), it provides anti-inflammatory and antiproliferative effects to reduce psoriasis symptoms. This combination medication is applied topically and is prescribed for adult patients with moderate to severe plaque psoriasis.

Quick summary

Calcipotriene is a topical psoriasis treatment that works as a vitamin D3 analog to slow skin cell growth and reduce scaling.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy

Key facts at a glance

ATC
D05AX02
RxNorm
29365
Generic
Calcipotriene
Class
atc-d05
Brands
Calcitrene, Sorilux, Enstilar, Dovonex, Wynzora, Pellix, Taclonex
Availability
rx
Lactation
unknown
Routes
topical
Forms
ointment, cream, solution
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
500mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
250mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
400mg daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity - ingestion of large amounts of topical preparation could lead to systemic absorption and vitamin D toxicity
Chronic overdose: Prolonged excessive topical application leading to hypercalcemia - cumulative effects from continuous use exceeding recommended amounts over weeks to months
Immediate actions
Gastric lavage if ingestion within 1-2 hours, activated charcoal may be administered, monitor serum calcium levels, intravenous fluids, discontinue topical application
Antidote
No specific antidote exists - treatment is supportive and addresses hypercalcemia(N/A - no specific antidote; management focuses on reducing calcium levels and supporting organ function)
Poison Control: 1-800-222-1222

Special Populations

11 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid use during first trimester unless benefits outweigh risks

Monitor

regular prenatal care

Use with caution and monitor for adverse effects.

⚠

pregnancy

second trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

use only if benefits outweigh potential risks

Monitor

routine prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

use lowest effective dose

Key Recommendations

avoid extensive body surface area application

Monitor

routine prenatal care

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

use smallest effective amount

Key Recommendations

avoid applying to breast area or use alternate feeding method

Monitor

monitor infant for hypercalcemia symptoms

Use with caution and monitor for adverse effects.

⚠

pediatric_age

children under 12
caution
FDA Category
C
Dose Adjustment

not recommended

Key Recommendations

not recommended for children under 12 years due to limited safety data

Monitor

close monitoring if used

Use with caution and monitor for adverse effects.

⚠

pediatric_age

adolescents 12 18
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

may be used with caution in adolescents with careful monitoring

Monitor

monitor for adverse effects

Use with caution and monitor for adverse effects.

✓

geriatric

elderly
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

safe for use in elderly patients with normal renal and hepatic function

Monitor

standard monitoring

✓

renal_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required due to minimal systemic absorption

Monitor

standard monitoring

✓

renal_impairment

severe
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required but monitor closely

Monitor

monitor renal function

✓

hepatic_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

no dosage adjustment required due to minimal systemic absorption

Monitor

standard monitoring

✓

hepatic_impairment

severe
safe
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

use with caution and monitor

Monitor

monitor hepatic function

Statistics and clinical data

prescribingFDA
2023

First FDA approval

Value:1994

Initial FDA approval year for calcipotriene topical solution (Dovonex)

drug_classWHO
2023

Drug class

Value:Synthetic vitamin D3 analog

ATC classification: L04AD02 (Immunosuppressants)

usageFDA
2023

Primary indication

Value:Plaque psoriasis treatment

Topical treatment for plaque psoriasis vulgaris

mechanismPubChem
2023

Mechanism of action

Value:Vitamin D receptor agonist

Binds to vitamin D receptors to regulate skin cell proliferation and differentiation

Treats plaque psoriasis vulgaris in adults, particularly effective for scalp and body plaques when combined with betamethasone dipropionate ointment or suspension.

Calcipotriene binds to vitamin D receptors in skin cells, regulating cell proliferation and differentiation. When combined with betamethasone, it provides complementary anti-inflammatory and immunosuppressive effects that reduce redness, scaling, and itching associated with psoriasis.

For topical use only; avoid contact with face, eyes, and mucous membranes. Not recommended for long-term continuous use due to corticosteroid component. May cause local irritation; use with caution in patients with hypercalcemia or impaired calcium metabolism. Pregnancy category C.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

WellAlly may earn a referral fee from linked resources at no extra cost to you. Editorial content is never influenced by commercial relationships.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy