SERDAEN- chlorhexidine diacetate soap

Serdaen by

Drug Labeling and Warnings

Serdaen by is a Otc medication manufactured, distributed, or labeled by Browne Hansen LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Chlorhexidine Diacetate 1%

INACTIVE INGREDIENT

Inactive Ingredients

Water, Cola Det SDC, Sodium Xylem Sulfate, Tocopheryl Acetate, Fragrance

PURPOSE

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses

Prevent overgrowth of bacteria prior to surgical procedure

Prevent recurrent bacterial infections

Prevent infections around superficial wounds

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help

or contact a poison control center right away.

WARNINGS

Warnings

For external use only.

Do not use:

If allergic to Chlorhexidine or other ingredients in formulation

In contact with the genital area

On wounds that exceed the superficial layer of skin.

WHEN USING

When using this product

Avoid eye contact. Should contact occur,

rinse thoroughly with water.

STOP USE

Discontinue use and consult a health care practitioner

if irritation or allergic reaction develops.

DOSAGE & ADMINISTRATION

Directions

Apply liberally to moistened area, wash and rinse thoroughly.

All product should be rinsed and dried immediately

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SERDAEN  
chlorhexidine diacetate soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56149-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE ACETATE	24 mg  in 3 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM SULFATE (UNII: 0YPR65R21J)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
MONOETHANOLAMINE (UNII: 5KV86114PT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56149-001-01	3 g in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/01/2013

Labeler - Browne Hansen LLC (962275843)