International reference: 1 US FDA recall for this ingredient

cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program. (desonide)

US-market enforcement records (OpenFDA), shown for reference - not specific to this product in Kenya.

Registered Kenya · PPB

DESONIDE CREAM

DESONIDE

H88279 DESONIDE 0.1% W/W dermatologicals INN generic

What it does

Desonide is a mild topical steroid used to reduce inflammation and relieve itching on the skin.

Commonly used for: skin rashes, eczema, dermatitis

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
H88279
Registration date
-
Expiry date
-
Status
Registered
Active ingredient
DESONIDE
Dosage form
DESONIDE 0.1% W/W
Strength
-
Pack size
-
Therapeutic class
-
ATC class (WHO)
D07AB - Corticosteroids, moderately potent (group II)
Drug group
DERMATOLOGICALS
RxNorm RxCUI
3254
Manufacturer / MAH
Laboratory & Allied
Applicant / LTR
-
Country of origin
LOCAL
Manufacturer location
National Park East gate road, Lab and, Mombasa Road, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 21:36:47 · updated 2026-07-20 11:11:07

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Desonide is a mild topical steroid used to reduce inflammation and relieve itching on the skin.

What it treats

  • skin rashes
  • eczema
  • dermatitis

How it works

Desonide works by calming down the immune response in the skin, which helps to reduce redness and swelling.

Who it's for

Desonide is for adults and children needing treatment for mild skin conditions.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: desonide

BNF-referenced

Desonide is a synthetic, nonfluorinated topical corticosteroid primarily used for its anti-inflammatory, antipruritic, and vasoconstrictive effects. It is indicated for the treatment of various dermatological conditions, helping to alleviate symptoms such as redness, itching, and swelling associated with inflammatory skin disorders.

Indications

  • Atopic dermatitis
  • Contact dermatitis
  • Psoriasis
  • Seborrheic dermatitis
  • Nummular eczema

Dosage

Children: Refer to the BNF for Children for appropriate dosing guidelines.

Adults: Apply a thin layer to the affected area once or twice daily, as directed by a healthcare professional.

Mechanism of action

Desonide exerts its effects by binding to cytosolic glucocorticoid receptors, forming a complex that migrates to the nucleus and interacts with genetic elements on DNA. This interaction leads to the activation and repression of specific genes. The anti-inflammatory action is thought to result from the induction of lipocortins, proteins that inhibit phospholipase A2, ultimately reducing the production of pro-inflammatory mediators like prostaglandins and leukotrienes by preventing the release of arachidonic acid from membrane phospholipids.

Pharmacodynamics

As a corticosteroid, desonide is effective in reducing inflammation and pruritus in various skin conditions. Its action as a topical agent allows for localized treatment with minimal systemic absorption, thus reducing the risk of systemic side effects typically associated with corticosteroids.

Pharmacokinetics

Desonide is primarily applied topically, which limits its systemic absorption. When used as directed, it demonstrates rapid onset of action at the site of application. The pharmacokinetics of desonide in terms of absorption, distribution, metabolism, and excretion are less documented due to its topical use, though systemic absorption is generally low compared to systemic corticosteroids.

Adverse effects

  • Burning sensation
  • Itching
  • Dryness
  • Skin atrophy
  • Striae
  • Hypopigmentation

Precautions

  • Avoid use on infected areas unless treated appropriately
  • Use with caution in patients with a history of hypersensitivity to corticosteroids
  • Long-term use may lead to systemic absorption and adrenal suppression

Pregnancy

Use during pregnancy only if the benefits outweigh the risks, as corticosteroids can potentially affect fetal development.

Breast-feeding

Desonide is excreted in breast milk; caution is advised when used by nursing mothers.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

  • Topical cream
  • Topical ointment
  • Topical lotion

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: desonide

PubChem CID 5311066

Molecular formula: C24H32O6

Mechanism of action

Like other topical corticosteroids, desonide has anti-inflammatory, antipruritic and vasoconstrictive properties. The drug binds to cytosolic glucocorticoid receptors. This complex migrates to the nucleus and binds to genetic elements on the DNA. This activates and represses various genes. However corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2.

Pharmacodynamics

Desonide is a synthetic nonfluorinated corticosteroid for topical dermatologic use. The corticosteroids constitute a class of primarily synthetic steroids used topically as anti-inflammatory and antipruritic agents.

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.

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