SulfaCleanse 8/4 description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

SulfaCleanse 8/4

PruGen, Inc.

SULFACLEANSE TM 8/4 TOPICAL SUSPENSION REV.1.0




FULL PRESCRIBING INFORMATION




Uses

SulfaCleanse™ 8/4 is indicated for the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

SulfaCleanse™ 8/4 is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. SulfaCleanse™ 8/4 is not to be used by patients with kidney disease.

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.

FOR EXTERNAL USE ONLY. Keep away from eyes. Keep out of reach of children. Keep container tightly closed.

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

Category C – Animal reproduction studies have not been conducted with SulfaCleanse™ 8/4. It is also not known whether SulfaCleanse™ 8/4 can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. SulfaCleanse™ 8/4 should be given to a pregnant woman only if clearly needed.

It is not known whether sodium sulfacetamide is excreted in the human milk following topical use of SulfaCleanse™ 8/4. 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 SulfaCleanse™ 8/4 is administered to a nursing woman.

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

Although rare, sodium sulfacetamide may cause local irritation.

Apply SulfaCleanse™ 8/4 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 SulfaCleanse™ 8/4 sooner or using less often.

SulfaCleanse™ 8/4 is available in a 16 fl. oz. (473 mL) bottle, NDC 42546-175-16.

Store at controlled room temperature 20°-25° C (68°-77° F); excursions permitted to 15°-30°C (59°-86°F).
Protect from freezing.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

NDC 42546-175-16

SulfaCleanseTM 8/4 (sodium sulfacetamide 8% and sulfur 4%)

Topical Suspension in a vehicle containing Green Tea and Aloe

Rx only

16 fl oz (473 ml)

PruGen, Inc. Pharmaceuticals

SulfaCleanse 8/4

SulfaCleanse 8/4

sodium sulfacetamide and sulfur LOTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:42546-175
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFACETAMIDE SODIUM SULFACETAMIDE 80 mg
SULFUR SULFUR 40 mg

Inactive Ingredients

Ingredient Name Strength
ALOE
BUTYLATED HYDROXYTOLUENE
CETYL ALCOHOL
DISODIUM OLEAMIDO MEA-SULFOSUCCINATE
EDETATE DISODIUM
GLYCERYL MONOSTEARATE
GREEN TEA LEAF
magnesium aluminum silicate
METHYLPARABEN
PEG-100 STEARATE
PROPYLPARABEN
water
SODIUM COCOYL ISETHIONATE
TAURINE
SODIUM THIOSULFATE
stearyl alcohol
XANTHAN GUM

Product Characteristics

Color
yellow

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 473 in 1 BOTTLE, PUMP
2 NDC:42546-175-16 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-05-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.