PUSH CLEAN- benzalkonium chloride cloth

Push Clean by

Drug Labeling and Warnings

Push Clean by is a Otc medication manufactured, distributed, or labeled by pushclean technology plastik sanayi ve ticaret limited sirketi, Push Clean US LLC, Ozsoy Organik Temizlik Urn. Ve End. Urn. Paz. San. Ve Tic. Ltd. Sti., PUSHCLEAN TECHNOLOGY PLASTIK SANAYI VE TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each wipe)

Benzalkonium Chloride 0.13% Purpose: Antiseptic

Purpose

Antiseptic

Use[s]

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only

Do not use

• in children less than 2 months of age
• on open skin wounds

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

• Place the container on a hard flat surface. Using your thumb, press and hold firmly in the center of the container for a second and release. Wait for the towelette to rise completely out of the container. Remove and unfold the towelette for use.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Avoid freezing and excessive heat above 40C (104F)
• Store between 20-25 C (68-77F)

Inactive ingredients

sodium hydroxide, water

PRINCIPAL DISPLAY PANEL

73737-436-10

INGREDIENTS AND APPEARANCE

PUSH CLEAN 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73737-436
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
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73737-436-10	4.5 mL in 1 BOX; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/30/2020

Labeler - Ozsoy Organik Temizlik Urn. Ve End. Urn. Paz. San. Ve Tic. Ltd. Sti. (503013069)

Establishment
Name	Address	ID/FEI	Business Operations
Ozsoy Organik Temizlik Urn. Ve End. Urn. Paz. San. Ve Tic. Ltd. Sti.		503013069	manufacture(73737-436)