Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension, In a vehicle containing Green Tea and Aloe

/Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension, In a vehicle containing Green Tea and Aloe
Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension, In a vehicle containing Green Tea and Aloe2018-09-06T09:12:40+00:00

Prescription Drug Name:

Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension, In a vehicle containing Green Tea and Aloe

ID:

6893220a-133b-f72e-e053-2991aa0a7037

Code:

34391-3

DESCRIPTION:


id: 6893220a-133d-f72e-e053-2991aa0a7037
displayName: DESCRIPTION SECTION
FDA Article Code: 34089-3

Sodium sulfacetamide is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically sodium sulfacetamide is N-[(4-aminophenyl) sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is: Each mL of Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension contains 80 mg of Sodium Sulfacetamide and 40 mg of Sulfur in a formulation containing purified water, sodium cocoyl isethionate, disodium oleamido MEA sulfosuccinate, green tea extract, cetyl alcohol, stearyl alcohol, glycerol stearate and PEG 100 stearate, methyl paraben, propyl paraben, butylated hydroxytoluene, aloe vera gel, sodium thiosulfate, disodium EDTA, magnesium aluminum silicate, xanthan gum, sodium methyl cocoyl taurate and white petrolatum.

CLINICAL PHARMACOLOGY:


id: 6893220a-133e-f72e-e053-2991aa0a7037
displayName: CLINICAL PHARMACOLOGY SECTION
FDA Article Code: 34090-1

The most widely accepted mechanism of action of sulfonamides is the Woods-Fildes theory, which is based on the fact that sulfonamides act as competitive antagonists to para-aminobenzoic acid (PABA), an essential component for bacterial growth. While absorption through intact skin has not been determined, sodium sulfacetamide is readily absorbed from the gastrointestinal tract when taken orally and excreted in the urine, largely unchanged. The biological half-life has variously been reported as 7 to 12.8 hours. The exact mode of action of sulfur in the treatment of acne is not known, but it has been reported that it inhibits the growth of Propionibacterium acnes and the formation of free fatty acids.

INDICATIONS:


id: 6893220a-133f-f72e-e053-2991aa0a7037
displayName: INDICATIONS & USAGE SECTION
FDA Article Code: 34067-9

Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

CONTRAINDICATIONS:


id: 6893220a-1340-f72e-e053-2991aa0a7037
displayName: CONTRAINDICATIONS SECTION
FDA Article Code: 34070-3

Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or ony other component of this preparation. Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension is not to be used by patients with kidney disease.

WARNINGS:


id: 6893220a-1341-f72e-e053-2991aa0a7037
displayName: WARNINGS SECTION
FDA Article Code: 34071-1

Although rare, sensitivity to sodium sulfacetaminde may occur. Therefore, caution and careful supervision should be observed when prescribing this drug for patients who may be prone to hypersensitivity to topical sulfonamides. Systemic toxic reactions such as agranulocytosis, acute hemolytic anemia, purpura hemorrhagica, drug fever, jaundice and contact dermatitis indicate hypersensitivity to sulfonamides. Particular caution should be employed if areas of denuded or abraded skin are involved. FOR EXTERNAL USE ONLY. Keep away from eyes. Keep out of reach of children. Keep container tightly closed.

PRECAUTIONS:


id: 6893220a-1342-f72e-e053-2991aa0a7037
displayName: GENERAL PRECAUTIONS SECTION
FDA Article Code: 34072-9

General – If irritation develops, use of the product should be discontinued and appropriate therapy instituted. Patients should be carefully observed for possible local irritation or sensitization during long-term therapy. The object of this therapy is to achieve desquamation without irritation, but sodium
sulfacetamide and sulfur can cause reddening and scaling of the epidermis. These side effects are not unusual in the treatment of acne vulgaris, but patients should be cautioned about the possibility.

Information for patients


id: 6893220a-1343-f72e-e053-2991aa0a7037
displayName: INFORMATION FOR PATIENTS SECTION
FDA Article Code: 34076-0

Avoid contact with eyes, eyelids, lips and mucous membranes. If accidental contact occurs, rinse with water. If excessive irritation develops, discontinue use and consult your physician.

Carcinogenesis, Mutagenesis and Impairment of Fertility


id: 6893220a-1344-f72e-e053-2991aa0a7037
displayName: CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION
FDA Article Code: 34083-6

Long-term studies in animals have not been performed to evaluate carcinogenic potential.

PREGNANCY:


id: 6893220a-1345-f72e-e053-2991aa0a7037
displayName: PREGNANCY SECTION
FDA Article Code: 42228-7

Category C. Animal reproduction studies have not been conducted with Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension. It is not known whether Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.
Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension should be given to a pregnant woman only if clearly needed.

NURSING MOTHERS:


id: 6893220a-1346-f72e-e053-2991aa0a7037
displayName: NURSING MOTHERS SECTION
FDA Article Code: 34080-2

It is not known whether sodium sulfacetamide is excreted in the human milk following topical use of Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension. However, small amounts of orally administered sulfonamides have been reported to be eliminated in human milk. In view of this and because many
drugs are excreted in human milk, caution should be exercised when Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension is administered to a nursing woman.

PEDIATRIC USE:


id: 6893220a-1347-f72e-e053-2991aa0a7037
displayName: PEDIATRIC USE SECTION
FDA Article Code: 34081-0

Safety and effectiveness in children under the age of 12 have not been established.

ADVERSE REACTIONS:


id: 6893220a-1348-f72e-e053-2991aa0a7037
displayName: ADVERSE REACTIONS SECTION
FDA Article Code: 34084-4

Although rare, sodium sulfacetamide may cause local irritation.

DOSAGE AND ADMINISTRATION:


id: 6893220a-1349-f72e-e053-2991aa0a7037
displayName: DOSAGE & ADMINISTRATION SECTION
FDA Article Code: 34068-7

Apply Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension once or twice daily to affected areas, or as directed by your physician. Wet skin and liberally apply to areas to be cleansed. Massage gently into skin for 10-20 seconds, working into a full lather, rinse thoroughly and pat dry. If drying occurs, it may be controlled by rinsing off Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension sooner or using less often.

HOW SUPPLIED:


id: 6893220a-134a-f72e-e053-2991aa0a7037
displayName: HOW SUPPLIED SECTION
FDA Article Code: 34069-5

Sodium Sulfacetamide 8% – Sulfur 4% Topical Suspension is available in 16 fl oz (473 mL) bottles, NDC 42192-133-16.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


id: 6893220a-134d-f72e-e053-2991aa0a7037
displayName: PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA Article Code: 51945-4

NDC 42192-133-16 Sodium Sulfacetamide 8% –

Sulfur 4% Topical Suspension
In a vehicle containing

Green Tea and Aloe
Rx Only SHAKE WELL 16 fl. oz. (473 mL) Acella

PHARMACEUTICALS, LLC