WIPE OUT LAVENDER SCENT ANTIBACTERIAL- benzalkonium chloride spray

WIPE OUT Lavender Scent ANTIBACTERIAL by

Drug Labeling and Warnings

WIPE OUT Lavender Scent ANTIBACTERIAL by is a Otc medication manufactured, distributed, or labeled by TZUMI INNOVATIONS LLC, Xiamen Tesimeier Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

■ To decrease bacteria on the skin that could cause disease

WARNINGS

For external use only. Flammable.

When using this product,

keep out of eyes. In case of contact with eyes, flush thoroughly with water

Avoid contact with broken skin

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

Hold can upright 6"-8" from hand. 

Spray 3-4 seconds until covered with mist

For children under 6, use only under adult supervision

Not recommended for infants

Other Information

Contents under pressure

Keep away from heat, sparkles, and open flame

Do not puncture or incinerate container

keep in dry, cool and well ventilated place

Recommended storage temperature: 32F-104F (0-40C)

Inactive ingredients

Aloe Barbadensis Leaf Etract, Fragrance, Glycerin, Phenoxyethanol, Tocopheryl Acetate, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WIPE OUT LAVENDER SCENT ANTIBACTERIAL 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77878-018
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)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77878-018-01	710 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/07/2020

Labeler - TZUMI INNOVATIONS LLC (117426322)

Establishment
Name	Address	ID/FEI	Business Operations
Xiamen Tesimeier Biotechnology Co., Ltd.		550462445	manufacture(77878-018)