KENDALL ANTIMICROBIAL CLEANSER- benzalkonium chloride liquid

Kendall Antimicrobial Cleanser by

Drug Labeling and Warnings

Kendall Antimicrobial Cleanser by is a Otc medication manufactured, distributed, or labeled by Covidien Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.13%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use

• a no-rinse topical antiseptic that protects against microbial contamination
• ideal for chapped or lightly traumatized skin
  

WARNINGS

Warnings

For external use only.

When using this product 

• do not get into eyes
  

Do not use on 

• deep or puncture wounds
• animal bites
• serious burns
  

Stop use and ask a doctor if condition worsens or symptoms last more than seven days.

Keep out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

Directions

• spray soiled or odorous areas
  
• gently wipe clean. Repeat as necessary.
• pat dry.  No rinse necessary.
  
• apply Kendall Moisturizing Lotion, Moisture Barrier Cream or Soothing Ointment as necessary
  

SPL UNCLASSIFIED SECTION

Other Information

• protect from freezing
• avoid excessive heat
  

INACTIVE INGREDIENT

Inactive ingredients

Water, Polysorbate 20, linoleamidopropyl PG-dimonium chloride phosphate, propylene glycol, cirtus aurantium bergamia (bergamot) fruit oil, citrus medica vulgaris peel oil, retinyl palmitate, tocopheryl acetate, methylparaben, propylparaben, diazolidinyl urea

QUESTIONS

Questions or comments?  1-800-962-9888

PRINCIPAL DISPLAY PANEL

Image of 4 Ounce Label

INGREDIENTS AND APPEARANCE

KENDALL ANTIMICROBIAL CLEANSER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 28851-691
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.13 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHOSPHATE ION (UNII: NK08V8K8HR)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BERGAMOT OIL (UNII: 39W1PKE3JI)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ACETATE ION (UNII: 569DQM74SC)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 28851-691-01	118 mL in 1 BOTTLE, SPRAY
2	NDC: 28851-691-02	236 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	04/05/2011

Labeler - Covidien Inc. (805770828)