Hydrocortisone And Iodoquinol
Generic Name: hydrocortisone and iodoquinol
Brand Names:
Hydrocortisone Iodoquinol
DESCRIPTION Each gram contains 10 mg of hydrocortisone and 10 mg of iodoquinol in a vehicle consisting of: cetyl alcohol, glycerin, glyceryl stearate SE, mineral oil, PEG-100 stearate, phenoxyethanol, purified water, stearyl alcohol, white petrolatum, xanthan gum. Paraben Free.
Overview
DESCRIPTION Each gram contains 10 mg of hydrocortisone and 10 mg of iodoquinol in a vehicle consisting of: cetyl alcohol, glycerin, glyceryl stearate SE, mineral oil, PEG-100 stearate, phenoxyethanol, purified water, stearyl alcohol, white petrolatum, xanthan gum. Paraben Free.
Uses
INDICATIONS Based on a review of a related drug by the National Research Council and subsequent FDA classification for that drug, the indications are as follows: "Possibly" Effective: Contact or atopic dermatitis; impetiginized eczema; nummular eczema; endogenous chronic infectious dermatitis; stasis dermatitis; pyoderma; nuchal eczema and chronic eczematoid otitis externa; acne urticata; localized or disseminated neurodermatitis; lichen simplex chronicus; anogenital pruritus (vulvae, scroti, ani); folliculitis; bacterial dermatoses; mycotic dermatoses such as tinea (capitis, cruris, corporis, pedis); moniliasis; intertrigo. Final classification of the less-than-effective indications requires further investigation.
Dosage
DOSAGE AND ADMINISTRATION Apply to affected area 3 to 4 times daily in accordance with physician's directions.
Side Effects
ADVERSE REACTIONS The following local adverse reactions are reported infrequently with topical corticosteroids. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infections, skin atrophy, striae and miliaria.
Warnings
WARNING FOR EXTERNAL USE ONLY. CONTRAINDICATIONS This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.
Pregnancy
Pregnancy Category C Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.
Storage
STORAGE Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (between 59°F to 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized. Keep container tightly closed. NOTICE Protect from freezing and excessive heat.
Frequently Asked Questions
What is Hydrocortisone And Iodoquinol used for?▼
INDICATIONS Based on a review of a related drug by the National Research Council and subsequent FDA classification for that drug, the indications are as follows: "Possibly" Effective: Contact or atopic dermatitis; impetiginized eczema; nummular eczema; endogenous chronic infectious dermatitis; stasis dermatitis; pyoderma; nuchal eczema and chronic eczematoid otitis externa; acne urticata; localized or disseminated neurodermatitis; lichen simplex chronicus; anogenital pruritus (vulvae, scroti, ani); folliculitis; bacterial dermatoses; mycotic dermatoses such as tinea (capitis, cruris, corporis, pedis); moniliasis; intertrigo. Final classification of the less-than-effective indications requires further investigation.
What are the side effects of Hydrocortisone And Iodoquinol?▼
ADVERSE REACTIONS The following local adverse reactions are reported infrequently with topical corticosteroids. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infections, skin atrophy, striae and miliaria.
Can I take Hydrocortisone And Iodoquinol during pregnancy?▼
Pregnancy Category C Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.
What are the important warnings for Hydrocortisone And Iodoquinol?▼
WARNING FOR EXTERNAL USE ONLY. CONTRAINDICATIONS This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.
Related Medications
Alpha Lipoic Acid, Arnica Montanaroot,sus Scrofa Cartilage,coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo,sus Scrofa Umbilical Cord,nadide,sodium Diethyl Oxalacetate, Sus Scrofa Placenta,toxicodendron Pubescens Leaf,sanguinaria Canadensis Root,silicon Dioxide,sulfur,comfrey Root
alpha lipoic acid, arnica montanaroot,sus scrofa cartilage,coenzyme a, solanum dulcamara top, sus scrofa embryo,sus scrofa umbilical cord,nadide,sodium diethyl oxalacetate, sus scrofa placenta,toxicodendron pubescens leaf,sanguinaria canadensis root,silicon dioxide,sulfur,comfrey root
Dosage form: TABLET. Active ingredients: ALPHA LIPOIC ACID (6 [hp_X]/1); ARNICA MONTANA ROOT (1 [hp_X]/1); COENZYME A (6 [hp_X]/1); COMFREY ROOT (8 [hp_X]/1); NADIDE (6 [hp_X]/1); SANGUINARIA CANADENSIS ROOT (3 [hp_X]/1); SILICON DIOXIDE (6 [hp_X]/1); SODIUM DIETHYL OXALACETATE (6 [hp_X]/1); SOLANUM DULCAMARA TOP (2 [hp_X]/1); SULFUR (6 [hp_X]/1); SUS SCROFA CARTILAGE (4 [hp_X]/1); SUS SCROFA EMBRYO (4 [hp_X]/1); SUS SCROFA PLACENTA (4 [hp_X]/1); SUS SCROFA UMBILICAL CORD (4 [hp_X]/1); TOXICODEN
Calendula Officials Flowers
calendula officials flowers
Purpose Section Skin Protectant
Naloxone Hcl Dihydrate
naloxone hcl dihydrate
Dosage form: POWDER. Active ingredients: NALOXONE HYDROCHLORIDE DIHYDRATE (1 kg/kg). Category: BULK INGREDIENT.
Medical Disclaimer
This drug information is for educational purposes only and should not replace professional medical advice. Drug information is sourced from the FDA National Drug Code Directory and Structured Product Labeling. Always consult with a healthcare provider before starting, stopping, or changing any medication.