ZEP HANDSTAND ANTIMICROBIAL- benzalkonium chloride liquid

Zep Handstand Antimicrobial by

Drug Labeling and Warnings

Zep Handstand Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Zep Inc., Kutol Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial handwashing

Uses

Handwash to help decrease bacteria on the skin.

Warnings

For external use only.

Do not use

Do not use in the eyes. In case of eye contact, immediately flush with water.

Stop use and ask a doctor

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children

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

Directions

• Apply a small amount, covering hands with product for 30 seconds. Add water, lather and rinse.
• Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

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

QUESTIONS

1-877-I-BUY-ZEP/1-877-428-9937

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP HANDSTAND ANTIMICROBIAL 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-127
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURIMINODIPROPIONATE (UNII: 7G447D0DH9)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SORBITOL (UNII: 506T60A25R)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-127-01	9600 mL in 1 CASE; Type 0: Not a Combination Product	08/23/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/23/2017

Labeler - Zep Inc. (030471374)