WIPE OUT ANTIBACTERIAL LIQUID HAND LAVENDER SCENT- benzalkonium chloride soap

WIPE OUT ANTIBACTERIAL Liquid Hand lavender scent by

Drug Labeling and Warnings

WIPE OUT ANTIBACTERIAL Liquid Hand lavender scent by is a Otc medication manufactured, distributed, or labeled by TZUMI INNOVATIONS LLC, Aogrand International Trade Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride  0.13%

Purpose

Antibacterial

Use

For hand washing to decrease bacteria on the skin

Warnings

For external use only

WHEN USING

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water

STOP USE

Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours

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.

Directions

• Wet hands 
• Apply palmful to hands
• Scrub thoroughly for at least 15 seconds
• Rinse thoroughly and dry

Inactive ingredients

Water, Cocamidopropyl dimethylamine oxide, Citric Acid, Fragrance, Kathon, Glycerin, Fatty acyl diethanol amine, Disodium EDTA, Hydroxyethyl Cellulose (250HHR), Blue 1 (CI 42090), CI 18134

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WIPE OUT ANTIBACTERIAL LIQUID HAND LAVENDER SCENT 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77878-029
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
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
DISODIUM HEDTA (UNII: KME849MC7A)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77878-029-01	221 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/23/2020

Labeler - TZUMI INNOVATIONS LLC (117426322)

Establishment
Name	Address	ID/FEI	Business Operations
Aogrand International Trade Corporation		421353092	manufacture(77878-029)