Microplastics and Misinformation: What Science Really Says
November 12, 2025
Brand Name :
Lyderm, Topsyn, Vanos, Lidemol, Topactin, Lidex, Tiamol
Synonyms :
fluocinonide
Class :
Topical Corticosteroids
Dosage Forms & StrengthsÂ
Ointment/topical solution/gelÂ
0.05%Â Â
CreamÂ
0.05%Â
0.1%Â
Â
Apply a slight coating topically once daily or every 12 hours as needed
Apply a slight coating topically once daily or every 12 hours as needed
Corticosteroid-responsive DermatosesÂ
Apply a slight coating topically once daily or every 12 hours as needed
Apply a small layer topically to the afflicted regions each day
Dosage Forms & StrengthsÂ
Ointment/topical solution/gelÂ
0.05%Â Â
CreamÂ
0.05%Â
0.1%Â
Corticosteroid-responsive DermatosesÂ
Apply a slight coating topically once daily or every 12 hours as needed
Refer adult dosingÂ
may decrease the anti-neoplastic effect of corticosteroids
may increase the tacrolimus immunosuppressive effect
may decrease the antineoplastic effect of flurandrenolide
antacids: they may diminish the bioavailability of corticosteroids K1
antacids: they may diminish the bioavailability of corticosteroids K1
may increase the immunosuppressive effect of immunosuppressive agents
may increase the serum concentration
may increase the serum concentration
bazedoxifene/conjugated estrogens
may increase the serum concentration
may increase the serum concentration
may increase the serum concentration
may increase the risk of adverse effects
may increase the risk of adverse effects
may increase the risk of adverse effects
may increase the risk of adverse effects
may increase the risk of adverse effects
When fluocinonide is used in combination with profenamine, this leads to reduction in therapeutic effectiveness of profenamine
may increase the hypokalemic effect of amphotericin
may decrease the bioavailability
may decrease the bioavailability
may decrease the bioavailability
may decrease the bioavailability
may decrease the bioavailability
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may enhance the adverse/toxic effect
may decrease the anti-neoplastic effect of each other when combined
When fluocinonide is used together with lomitapide, this leads to an enhancement in lomitapide’s metabolism
When fluocinonide is used together in combination with profenamine, this leads to reduction in therapeutic effectiveness of profenamine
When fluocinonide is aided by androstenediol, that promotes an increased risk of edema
Actions and Spectrum:Â
fluocinonide is a high-potency synthetic corticosteroid that is an anti-inflammatory and anti-pruritic agent when applied topically. It has a selective and potent action on the glucocorticoid receptor, leading to the formation of a glucocorticoid-receptor complex that translocates to the nucleus of the target cells. The complex modulates gene expression in the nucleus, leading to decreased production of pro-inflammatory cytokines and chemokines and increased production of anti-inflammatory proteins.Â
The overall mechanism of action of fluocinonide can be summarized as follows:Â
fluocinonide is effective against a broad spectrum of skin disorders, including:Â
An eczema is a group of skin conditions that cause the skin to become dry, itchy, and inflamed.Â
Frequency not definedÂ
StriaeÂ
Pigmentation changesÂ
Intracranial hypertensionÂ
Maceration of the skinÂ
FolliculitisÂ
Cushing’s syndromeÂ
HyperglycemiaÂ
IrritationÂ
Skin atrophyÂ
Acneform lesionsÂ
HPA suppression (with higher potency used >2 wk)Â
HypopigmentationÂ
MiliariaÂ
HyperglycemiaÂ
TelangiectasiaÂ
BurningÂ
GlycosuriaÂ
Contraindications/caution:Â
Contraindications:Â
Caution:Â
Pregnancy consideration: CÂ
Lactation: Excretion of the drug in human breast milk is unknownÂ
Pregnancy category:Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.  Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:Â
fluocinonide is a potent synthetic corticosteroid with anti-inflammatory, anti-pruritic, and vasoconstrictive properties. It exerts its pharmacological effects by binding to intracellular glucocorticoid receptors, leading to the inhibition of pro-inflammatory cytokines and the activation of anti-inflammatory genes. This action leads to the suppression of the immune response and the reduction of inflammation, swelling, redness, and itching.Â
Pharmacodynamics:Â
Pharmacokinetics:Â
AbsorptionÂ
fluocinonide is rapidly absorbed through the skin when applied topically. Occlusions, such as plastic wrap or an occlusive dressing can enhance its absorption.Â
DistributionÂ
After absorption, fluocinonide is distributed throughout the body. However, due to its high potency, only small amounts of the drug are required to achieve therapeutic effects. The drug binds strongly to plasma proteins, and the body’s metabolic processes influence its distribution.
MetabolismÂ
fluocinonide undergoes extensive metabolism in the liver, converting it into various metabolites. These metabolites are then excreted from the body.Â
Elimination and ExcretionÂ
The metabolites of fluocinonide are primarily excreted in the urine, with a small amount being excreted in the feces. The drug has a relatively short elimination half-life of approximately 2.5 hours.Â
Administration:Â
fluocinonide is a prescription medication available in different forms, such as creams, ointments, gels, and solutions for topical application. The appropriate method of administration will depend on the condition being treated and the severity of the symptoms. Here are some general guidelines for the administration of fluocinonide:Â
Patient information leafletÂ
Generic Name: fluocinonideÂ
Pronunciation: [ FLOO-oh-SIN-oh-nide ]Â
Why do we use fluocinonide?Â
fluocinonide is a potent synthetic corticosteroid primarily used to treat various skin conditions that cause inflammation, itching, and discomfort. Here are some of the most common uses of fluocinonide:Â