PERIFOAM- benzethonium chloride solution

Perifoam by

Drug Labeling and Warnings

Perifoam by is a Otc medication manufactured, distributed, or labeled by Sage Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses

PeriFoam™ is a safe, non-stinging foaming cleanser, which effectively kills odors and microorganisms on the skin, including the perineal area and around stoma sites and gastro-intestinal tube entry paints. PeriFoam™ will not bum or cause discomfort on irritated or tender skin, but will gently soften and moisturize as it cleans.

Warnings

For external use only. Discontinue use ~ irritation and redness develop.

If condition persists for more than 48 hours, consult a doctor.

Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance.

Directions

For Perineal Area and Around Stoma Site

Spray PeriFoam™ on the perineal area or stoma site. Remove excess debris quickly. Spray PeriFoam™ again and gently wipe with water dampened cloth. Rinse with water:

For Gastro-Intestinal Tube Sites

Spray PeriFoam™ around the entry site. Gently clean with a damp cloth. Rinse with water. Repeat as necessary. After cleaning the area. Apply SkinSeal™skin protectant around the site as directed by label.

Ingredients

Active Ingredient

Benzethonium Chloride, 0.2

Other Ingredients

purified water, non-ionic surtactants, fragrance, polyaminopropyl biguanide, aloe vera, dexpanthenol, disodium EDTA, and vitamin E.

STORAGE AND HANDLING

Store between 59"-86" F (15-30°C)

SPL UNCLASSIFIED SECTION

Manufactured By:
Sage Pharmaceuticals, Inc.
Shreveport, LA 71109

PRINCIPAL DISPLAY PANEL - 237ml Bottle Label

NDC: 59243-110-08

PeriFoam™
ANTI-BACTERIAL FOAMING CLEANSER

Active Ingredient: Benzethonium Chloride, 0.2%

REDUCES ODOR AND CONTAINS NO DYES

For foaming action, pull out tip of spray nozzle.

SHAKE WELL BEFORE USING

NET CONTENTS: 8 FL. OZ. (237ml)

INGREDIENTS AND APPEARANCE

PERIFOAM 
benzethonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59243-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POLOXAMER 188 (UNII: LQA7B6G8JG)
POLIHEXANIDE (UNII: 322U039GMF)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHERSOLAN (UNII: O03S90U1F2)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CAPRIC DIETHANOLAMIDE (UNII: SHH19DQ1DH)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59243-110-08	237 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	11/21/2000

Labeler - Sage Pharmaceuticals, Inc. (626120919)