Benzalkonium Chloride 0.13%

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease
Recommended for repeated use

Warnings: For external use only

Flammable: Keep away from heat and flame

Keep out of eyes

In case of contact with eyes, flush thoroughly with water

Avoid contact with broken skin

Do not inhale or ingest

Stop use and ask a doctor

if irritation or redness develops
Condition persists for more than 72 hours

If swallowed, get medical help or contact a poison control center right away

Wet hands thoroughly with product and allow to dry without wiping
Not recommended for infants

Other information

Do not store above 105°F
May discolor some fabrics harmful to wood finishes and plastics

Aloe leaf juice 0.3%, water(aqua)

DERMATOLOGIST TESTED

PARABEN FREE

SOOTHING ALOE VERA

KILL 99.9% OF GERMS

ALCOHOL FREE

60 SOFT WIPES

TO OPEN PACKAGE

Flip open dispensing cap
Locate wipe at center of rolland thread through small opening in lid
For best results dispense wipes at angle
When finished, snap lid acap shut to retain moisture

For use at home, at work, ro on-the-go.

DO NOT USE BEFORE AND AFTER EATING

Feature & details:

• Helps reduce the risk of infections

• Leaves no stickiness or residue on hands

• Removes light soils and dirt from hands

Manufactured by Shandong Fengrui Biotechnology Co., Ltd.

Manufactured in No.168, Qingwei Road, Dongliuting Community, Liuting sub-district, Qingdao, CHN

DO NOT FLUSH

NDC 80832-001-01

label of Benzalkonium Chloride sanitizing wipes NDC 80832-001-01

BBTIME HAND SANITIZING WIPES
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:80832-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	13 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:80832-001-01	7.8 g in 1 PACKAGE; Type 0: Not a Combination Product	10/12/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	10/12/2020

Labeler - Qingdao Fengrui Biotechnology Co., Ltd. (417156545)

Registrant - Qingdao Fengrui Biotechnology Co., Ltd. (417156545)

Name	Address	ID/FEI	Business Operations
Establishment
Qingdao Fengrui Biotechnology Co., Ltd.		417156545	label(80832-001) , manufacture(80832-001)