Cutar (coal tar)
Coal Tar Products Topical Emulsion
Last reviewed · Source: First Databank (FDB) drug data
Overview
Coal tar has keratoplastic and mild local irritant properties.
Coal tar preparations are used topically alone or in combination with other drugs (e.g., salicylic acid, sulfur) for controlling dandruff, seborrheic dermatitis, or psoriasis. Although there are few well-controlled studies demonstrating their efficacy, coal tar preparations are used and generally considered effective for relieving the itching and scalp flaking associated with dandruff; for relieving the itching, irritation, and skin flaking associated with seborrheic dermatitis; and for relieving the itching, redness, and scaling associated with psoriasis. However, patient acceptance of coal tar is very poor because it is extremely messy, malodorous, and stains skin and hair, and coal tar preparations have largely been replaced for many of these uses by other agents (e.g., topical antifungal agents, topical corticosteroids).
Although coal tar has been further modified or refined to potentially provide more esthetically acceptable and pharmaceutically practical preparation, there currently are no published data showing that these modified or refined preparations of coal tar are superior to or even equal in clinical efficacy to coal tar.
Generic name: coal tar
Pronunciation: (kole-tar)
Drug class: Coal Tar Products
Therapeutic class: Dermatological
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
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Indications
The following indications are listed for Cutar:
- Dandruff
- Psoriasis
- Seborrheic Dermatitis
Also known as: Branny Tetter, Dermatitis Seborrheica, Dyssebacea, Dyssebacia, Pityriasis Capitis, Pityriasis Sicca, Pityriasis Simplex, Scurf, Seborrhea Corporis, Seborrhea Furfuracea, Seborrhea Sicca, Seborrheic Eczema, Unna's Disease.
Dosing
Dosage of various coal tar preparations is not well established since well defined standards for specific contents of these preparations currently do not exist. (See Chemistry and Stability: Chemistry.)
For relief of itching and scalp flaking associated with dandruff; itching, irritation, and skin flaking associated with seborrheic dermatitis of the scalp; or itching, redness, and scaling associated with psoriasis of the scalp, coal tar preparations intended for use as a shampoo should be applied to wet hair and massaged vigorously into the scalp. Then, the scalp is rinsed thoroughly and application of the lotion and rinsing is repeated. Coal tar preparations intended for use as a shampoo usually are used twice weekly.
When coal tar preparations are used as a bath for relief of signs and symptoms associated with psoriasis or seborrheic dermatitis of the body or other dermatologic conditions of the body, an appropriate amount of these preparations should be diluted in lukewarm bath water. The coal tar preparation should be thoroughly mixed throughout the bath water. The patient should immerse himself into the bath and soak for 10-20 minutes. Bathing with a coal tar preparation may be performed once daily to once every 3 days; the usual duration of therapy is 30-45 days. If the physician prescribes the Goeckerman treatment (coal tar and phototherapy) for psoriasis, all of the coal tar preparation should be removed from the skin prior to exposure to radiation. Phototherapy may begin 2-72 hours after bathing with the coal tar preparation. A determination of the minimum phototoxic dose (MPD) of UVB, UVA, or UVA/B radiation should be made by the physician for each patient; the initial dosage of radiation should be suberythemal and should not exceed the MPD. The usual cautions associated with Goeckerman therapy should be followed. (See Cautions: Precautions and Contraindications.)
When coal tar preparations are applied directly to the skin for relief of signs and symptoms of psoriasis or seborrheic dermatitis of the body or other dermatologic conditions of the body, the coal tar preparation usually is applied topically to the affected area 1-4 times daily. When a coal tar preparation is applied once daily, it may be preferable to apply the preparation at bedtime. Coal tar preparations should be gently massaged into the area of application. After several minutes, any excess amount of the preparation should be removed with tissues. Removing excess amounts of the preparation may minimize staining of the skin and clothing. Once the condition has been controlled, it may be possible to decrease the frequency of application to 2 or 3 times weekly. If dryness of the skin occurs during use of the gel, an emollient may be applied to the treated area 1 hour after application of the coal tar gel or coal tar extract gel. If the physician prescribes the Goeckerman treatment for psoriasis, the coal tar preparation is applied once or twice daily at bedtime and/or at least 30-60 minutes prior to UV radiation. All of the coal tar preparation should be removed from the skin prior to radiation. The dosage of UV radiation must be individualized for each patient by the physician. The usual cautions associated with Goekerman therapy should be followed. (See Cautions: Precautions and Contraindications.)
Coal tar preparations are applied topically to the scalp as a shampoo or to the skin as a bath, cake, cream, gel, lotion, ointment, or solution. Coal tar preparations are for external use only and contact with the eyes should be avoided. (See Cautions: Precautions and Contraindications.) Coal tar preparations should not be applied in or near the anogenital area unless otherwise directed by a physician. (See Cautions: Carcinogenicity.)
No dosing information is available for this tab.
No dosing information is available for this tab.
Drug interactions
Although no known drug interactions have been reported to date, it is recommended that coal tar preparations not be used concomitantly with drugs (e.g., tetracyclines, psoralens, tretinoin) having phototoxic and/or photoactivating potential.
There are no contraindication interactions for this drug.
Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
Coal Tar/Cyclosporine
SEVERITY LEVEL: 2-Severe Interaction: Action is required to reduce the risk of severe adverse interaction.
MECHANISM OF ACTION: Concurrent use of cyclosporine and coal tar may result in excessive immunosuppression.(1)
CLINICAL EFFECTS: Concurrent use of cyclosporine and coal tar may increase the risk of skin malignancy.(1)
PREDISPOSING FACTORS: None determined.
PATIENT MANAGEMENT: The US manufacturer of cyclosporine states that concurrent use of cyclosporine and coal tar is contraindicated in psoriasis patients because of the possibility of increased risk of malignancies.(1)
DISCUSSION: Tumors have been reported in 32 (2.2%) of 1439 psoriasis patients treated with cyclosporine in clinical trials. Tumors have been reported in an additional 7 patients in post-marketing reports. Sixteen of these reports involved skin malignancies. Coal tar was used by 3 of the patients.(1)
There are no moderate interactions for this drug.
Contraindications
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There are no contraindication contraindications for this drug.
- Folliculitis
- Large open wound
There are no moderate contraindications for this drug.
Adverse reactions
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There are no severe adverse reactions for this drug.
Less Frequent
- Skin photosensitivity
Rare or Very Rare
- Dermatitis due to topical drug
- Folliculitis
- Skin irritation
- Skin rash
Precautions
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No enhanced messaging available.
Animal reproduction studies have not been performed with coal tar preparations. It is not known whether coal tar preparations can cause fetal harm when used topically by pregnant women. Coal tar preparations should be used during pregnancy only when clearly needed.
It is not known whether topically applied coal tar is absorbed and/or distributed into milk. Because of the potential for serious adverse reactions (i.e., carcinogenicity) from coal tar preparations in nursing infants, a decision should be made whether to discontinue nursing or the drug, taking into account the importance of the drug to the woman.
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ICD codes
| Code | Type | Description |
|---|---|---|
| Dandruff | ||
| L21.0 | ICD10CM | Seborrhea capitis |
| Psoriasis | ||
| L40 | ICD10CM | Psoriasis |
| L40.0 | ICD10CM | Psoriasis vulgaris |
| L40.1 | ICD10CM | Generalized pustular psoriasis |
| L40.2 | ICD10CM | Acrodermatitis continua |
| L40.3 | ICD10CM | Pustulosis palmaris et plantaris |
| L40.4 | ICD10CM | Guttate psoriasis |
| L40.5 | ICD10CM | Arthropathic psoriasis |
| L40.50 | ICD10CM | Arthropathic psoriasis, unspecified |
| L40.51 | ICD10CM | Distal interphalangeal psoriatic arthropathy |
| L40.52 | ICD10CM | Psoriatic arthritis mutilans |
| L40.53 | ICD10CM | Psoriatic spondylitis |
| L40.54 | ICD10CM | Psoriatic juvenile arthropathy |
| L40.59 | ICD10CM | Other psoriatic arthropathy |
| L40.8 | ICD10CM | Other psoriasis |
| L40.9 | ICD10CM | Psoriasis, unspecified |
| Seborrheic dermatitis | ||
| L21 | ICD10CM | Seborrheic dermatitis |
| L21.0 | ICD10CM | Seborrhea capitis |
| L21.1 | ICD10CM | Seborrheic infantile dermatitis |
| L21.8 | ICD10CM | Other seborrheic dermatitis |
| L21.9 | ICD10CM | Seborrheic dermatitis, unspecified |
ICD code information from First Databank (FDB).
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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