Sodium Sulfacetamide 10% and Sulfur 5% Cleanser

Manufacturer
Gabar Health Sciences Corp.
Effective date
2023-10-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:23:34

Label at a glance#

ProductSodium Sulfacetamide 10% and Sulfur 5% Cleanser
Active ingredientSULFACETAMIDE SODIUM, SULFUR
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rx Only

DESCRIPTION SECTION

DESCRIPTION: Each gram of Sodium Sulfacetamide and Sulfur (sodium sulfacetamide 10% w/w and sulfur 5% w/w) contains 100 mg of sodium sulfacetamide and 50 mg of colloidal sulfur in a vehicle consisting of: aloe vera leaf extract, butylated hydroxytoluene, cetyl alcohol, disodium oleamido monoethanolamine sulfosuccinate, edetate disodium, fragrance, glycerin, glyceryl monostearate, magnesium aluminum silicate, methylparaben, PEG-100 stearate, propylparaben, purified water, sodium cocoyl isethionate, sodium methyl cocoyl taurate, sodium thiosulfate, stearyl alcohol, xanthan gum.

Sodium sulfacetamide is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Sodium sulfacetamide is C 8H 9N 2NaO 3S·H 2O with molecular weight of 254.24. Chemically, it is N-[(4-aminophenyl)sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is:

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CLINICAL PHARMACOLOGY SECTION

CLINICAL PHARMACOLOGY


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 unknown, but it has been reported that it inhibits the growth of  Propionibacterium acnes and the formation of free fatty acids.

INDICATIONS & USAGE SECTION

INDICATIONS:

Sodium Sulfacetamide 10% & Sulfur 5% Cleanser is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

CONTRAINDICATIONS SECTION

CONTRAINDICATIONS:

Sodium Sulfacetamide 10% & Sulfur 5% Cleanser is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur, or any other component of this preparation. Sodium Sulfacetamide 10% & Sulfur 5% Cleanser is not to be used by patients with kidney disease.

WARNINGS SECTION

WARNING

Although rare, sensitivity to sodium sulfacetamide 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.


Sulfonamides are known to cause Stevens-Johnson syndrome in hypersensitive individuals. Stevens- Johnson syndrome also has been reported following the use of sodium sulfacetamide topically. Cases of drug induced systemic lupus erythematosus from topical sulfacetamide also have been reported. In one of these cases, there was a fatal outcome. KEEP OUT OF REACH OF CHILDREN.

PRECAUTIONS SECTION

PRECAUTIONSFOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE

SPL UNCLASSIFIED SECTION

General

If irritation develops, use of this product should be discontinued and appropriate therapy instituted. Patients should be very 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.

SPL UNCLASSIFIED SECTION

Carcinogenesis, Mutagenesis and Impairment of Fertility
Long-term studies in animals have not been performed to evaluate carcinogenic potential.

SPL UNCLASSIFIED SECTION

PREGNANCY
Category C
Animal reproduction studies have not been conducted with Sodium Sulfacetamide 9% & Sulfur 4.5% Wash. It is also not known whether Sodium Sulfacetamide 10% & Sulfur 5% Cleanser can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sodium Sulfacetamide 10% & Sulfur 5% Cleanser should be given to a pregnant woman only if clearly needed.

SPL UNCLASSIFIED SECTION

NURSING MOTHERS
It is not known whether Sodium Sulfacetamide is excreted in human milk following topical use of Sodium Sulfacetamide 10% & Sulfur 5% Cleanser. 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 10% & Sulfur 5% Cleanser is administered to a nursing woman.

SPL UNCLASSIFIED SECTION

PEDIATRIC USE
Safety and effectiveness in children under the age of 12 has not been established.

ADVERSE REACTIONS SECTION

ADVERSE REACTIONS


Although rare, sodium sulfacetamide may cause local irritation. Call your doctor for medical adviceabout side effects. To report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800- FDA-1088 or www.fda.gov/medwatch.

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION

Wash affected areas with Sodium Sulfacetamide 10%, and Sulfur 5% Cleanser one to two times daily, or as directed by your physician. Avoid contact with eyes or mucous membranes. Wet skin and liberally apply to areas to be cleansed, massage gently into skin for 10 to 20 seconds, working into a full lather, rinse thoroughly and pat dry. If drying occurs, it may be controlled by rinsing cleanser off sooner or using cleanser less often.

HOW SUPPLIED SECTION

HOW SUPPLIED

Sodium Sulfacetamide 10% & Sulfur 5% Cleanser is supplied in an 6oz. (170g) bottle (NDC 82429-107-06), 8oz. (227g) bottle (NDC 82429-107-08) and 12oz. (340g) bottle (NDC 82429-107-12) .


Store at 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (between 59°F and 86°F). See USP Controlled Room Temperature.


Note: Protect from freezing and excessive heat. The product may tend to darken slightly on storage. Slight discoloration does not impair the efficacy or safety of the product. Keep bottle packet tightly closed.


Occasionally, a slight yellowish discoloration may occur when an excessive amount of the product is used and comes in contact with white fabrics. This discoloration, however, presents no problem, as it is readily removed by ordinary laundering without bleaches.

SPL UNCLASSIFIED SECTION

Manufactured by:
Gabar Health Sciences,
Corp Atlanta, GA 30354 USA
Rev 04/23

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL - Bottle Label

Rx only
Sodium Sulfacetamide 10% & Sulfur 5% Cleanser
SHAKE WELL BEFORE USE

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82429-107SODIUM SULFACETAMIDE 10% AND SULFUR 5% CLEANSER (SULFACETAMIDE SODIUM AND SULFUR) RINSE [GABAR HEALTH SCIENCES CORP.]4Legacy NDC20231022_b954cee5-d1e6-405e-9946-e7b40aeee389.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
82429-107-06GM - Gram82429-107c6695667-94b9-404a-979e-0e25d094eff812023-05-05
82429-107-08GM - Gram82429-10753132e87-8603-4e08-a6f7-ffc82d3e135e12022-11-07
82429-107-12GM - Gram82429-10796f59f8a-59e9-48b9-b6eb-9dfe941cad1b12023-05-05

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82429-10782429-107-08, 82429-107-06, 82429-107-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4c2e11a2-b24c-d2c1-e063-6394a90a6415b954cee5-d1e6-405e-9946-e7b40aeee3892026-03-04Warnings, Adverse reactionsExact identifier
spl set id: b954cee5-d1e6-405e-9946-e7b40aeee389

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.