SODIUM SULFACETAMIDE, SULFUR description, usages, side effects, indications, overdosage, supplying and lots more!

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SODIUM SULFACETAMIDE, SULFUR

Austin Pharmaceuticals, LLC

Sodium Sulfacetamide 10% and Sulfur 5% Lotion


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Rx Only

DESCRIPTION:



89232

SODIUM SULFACETAMIDE, SULFUR

INDICATIONS:

CONTRAINDICATIONS:


CLINICAL PHARMACOLOGY:

WARNINGS AND PRECAUTIONS:

FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.



General:

Carcinogenesis, Mutagenesis and Impairment of Fertility:

Pregnancy: Pregnancy Category C.

Nursing Mothers:

Pediatric Use:

ADVERSE REACTIONS:

You should call your doctor for medical advice about side effects. To report a serious adverse event, call 1-855-899-4237.

DOSAGE AND ADMINISTRATION:


HOW SUPPLIED:





KEEP OUT OF REACH OF CHILDREN.


Austin Pharmaceuticals, LLC




SODIUM SULFACETAMIDE, SULFUR

SODIUM SULFACETAMIDE, SULFUR

SODIUM SULFACETAMIDE, SULFUR LOTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:42792-102
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SULFACETAMIDE SODIUM SULFACETAMIDE 100 mg
SULFUR SULFUR 50 mg

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
MEDIUM-CHAIN TRIGLYCERIDES
CETYL ALCOHOL
DIMETHICONE
EDETATE DISODIUM
GLYCERIN
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
PHENOXYETHANOL
METHYLPARABEN
BUTYLPARABEN
ETHYLPARABEN
PROPYLPARABEN
POLYACRYLAMIDE (1500 MW)
C13-14 ISOPARAFFIN
LAURETH-7
SODIUM THIOSULFATE
water
Zinc Oxide

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42792-102-01 25 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-04-30


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Be sure to consult your doctor before taking any medication!
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