Wednesday, May 16, 2012

Sodium Sulfacetamide




Dosage Form: lotion


Rx Only

DESCRIPTION:

Sulfacetamide sodium is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically sulfacetamide sodium is N-[(4-aminophenyl) sulfonyI]-acetamide, monosodium salt, monohydrate. The structural formula is:



Each gram of sulfacetamide sodium USP 10% and sulfur USP 5% contains 100 mg of Sodium Sulfacetamide USP and 50 mg of Sulfur USP in a cream containing: Benzyl Alcohol, Emulsifying Wax, Hamaelis virginiana (Witch Hazel) Distillate, Kaolin, Propanediol, Propylene Glycol, Purified Water, Quillaja (Quillaia) saponaria Extract, Silicon Dioxide, and Sodium Thiosulfate.



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, sulfacetamide sodium 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:

Sulfacetamide sodium and sulfur cleanser is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.



CONTRAINDICATIONS:

Sulfacetamide sodium and sulfur cleanser is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. Sulfacetamide sodium and sulfur cleanser is not to be used by patients with kidney disease.



WARNINGS:

Although rare, sensitivity to sulfacetamide sodium 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:

General - lf 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 sulfacetamide sodium 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 - 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 - Longterm studies in animals have not been performed to evaluate carcinogenic potential.



Pregnancy: Category C - Animal reproduction studies have not been conducted with sulfacetamide sodium and sulfur lotion. It is also not known whether sulfacetamide sodium and sulfur cleanser can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sulfacetamide sodium and sulfur cleanser should be given to a pregnant woman only if clearly needed.



Nursing Mothers - It is not known whether sulfacetamide sodium is excreted in the human milk following topical use of sulfacetamide sodium and sulfur lotion. 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 sulfacetamide sodium and sulfur cleanser is administered to a nursing woman.



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



ADVERSE REACTIONS:

Although rare, sulfacetamide sodium may cause local irritation.



DOSAGE AND ADMINISTRATION:

Use once daily or as directed by your physician. Wet skin. Apply in a film to entire face, avoiding contact with eyes or mucous membranes. Wait 10 minutes or until dry. Rinse thoroughly with water and pat dry.



HOW SUPPLIED:

Sulfacetamide sodium 10% and sulfur 5% cleanser is supplied in

6 oz (170 g) tube      NDC 67877-268-17

12 oz (340 g) bottle  NDC 67877-268-34


Store at 15°-25°C (59°-77°F).


Call your doctor about side effects. You may report side effects to FDA at 1-800-FDA-1088.


KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN


Rx Only


Manufactured for:

Ascend Laboratories, LLC

Montvale, NJ 07645


Manufactured by:

Crown Laboratories, Inc.

Johnson City, TN 37604



PRINTED IN USA                     P1815.01





ASCEND

Laboratories, LLC


NDC 67877-268-34


Sulfacetamide

Sodium

10%

& Sulfur

5%

Cleanser


Rx Only


NET WT 12oz

(340 g)










SULFACETAMIDE SODIUM, SULFUR 
sulfacetamide sodium, sulfur  lotion










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)67877-268
Route of AdministrationTOPICALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFACETAMIDE SODIUM (SULFACETAMIDE)SULFACETAMIDE SODIUM100 mg  in 1 g
SULFUR (SULFUR)SULFUR50 mg  in 1 g





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
167877-268-17170.1 g In 1 TUBENone
267877-268-34340.2 g In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/08/2011


Labeler - Ascend Laboratories, LLC (141250469)









Establishment
NameAddressID/FEIOperations
Crown Laboratories, Inc.079035945manufacture
Revised: 01/2012Ascend Laboratories, LLC




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