KIMBALL MIDWEST ANTIBACTERIAL HAND CLEANER- benzalkonium chloride liquid

KIMBALL MIDWEST Antibacterial Hand Cleaner by

Drug Labeling and Warnings

KIMBALL MIDWEST Antibacterial Hand Cleaner by is a Otc medication manufactured, distributed, or labeled by Kimball Midwest. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13% w/v

Purpose

Antibacterial Agent

Uses

To decrease bacteria on the skin.

Warnings

For external use only.

Avoid contact with eyes. If contact occurs, flush eyes with water. 

Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

Directions

Apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

Inactive Ingredients

Water, Cetrimonium Chloride, Lauramine Oxide, Sorbitol, Cocamide MEA, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Sodium Lauraminodipropionate, Citric Acid, Fragrance, Disodium EDTA, Methylisothiazolinone, Methychloroisothiazolinone, Yellow 5, Red 33.

SPL UNCLASSIFIED SECTION

Proven To Kill A Broad Spectrum Of Germs And Bacteria

Mild Yet Effective

Pleasant Spicy Floral Fragrance

Carefully read warnings on side panel

FOR INDUSTRIAL AND PROFESSIONAL USE ONLY

Manufactured for:
Kimball Midwest
4800 Roberts Rd.
Columbus, Ohio 43228
800-233-1294
www.kimballmidwest.com

DESCRIPTION
The Antibacterial Hand Cleaner is a fast-acting hand cleaner with a pleasant spicy floral fragrance. Kill germs without irritating the skin and helps prevent drying, cracking and chapping.

DIRECTIONS
Apply Antibacterial Hand Cleaner to wet hands. Work thoroughly into hands, knuckles and under fingernails. Rinse with water.

Made in the U.S.A.

Packaging

INGREDIENTS AND APPEARANCE

KIMBALL MIDWEST ANTIBACTERIAL HAND CLEANER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66608-216
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SORBITOL (UNII: 506T60A25R)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
SODIUM LAURIMINODIPROPIONATE (UNII: 7G447D0DH9)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66608-216-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/13/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/13/2024

Labeler - Kimball Midwest (017906231)