WIPE OUT ANTIBACTERIAL WIPES- benzalkonium chloride cloth

WIPE OUT Antibacterial Wipes by

Drug Labeling and Warnings

WIPE OUT Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG BINGER NONWOVEN CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiacterial

USE

To decrease bacteria on the
skin that could cause disease

Warning

For external use only.
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
■iritation and redness
develop■lcondition persists
for more than 72 houirs.

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

Directions

■I Wet hands thoroughly
with product and allow to dry
without wiping■I for children|
under 6, use only under
adult supervision
■not recommended for
infants
Other information
1 1 Keep containers tightly
closed in a dry, cool and
well-ventilated place.
■Recommended storage
temperature: 32°F to 104°F
(0°C to 40°C)

Inactive ingredients

aloe barbadensis leaf juice,
fragrance, phenoxyethanol,
polysorbate 20, propylene
glycol, tocopheryl acetate,
water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WIPE OUT ANTIBACTERIAL WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76896-003
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 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76896-003-05	60 in 1 BOTTLE	06/19/2020
1		4.9 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 76896-003-06	80 in 1 BOTTLE	06/19/2020
2		4.9 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 76896-003-01	10 in 1 BAG	06/19/2020
3		4.9 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 76896-003-02	20 in 1 BAG	06/19/2020
4		4.9 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 76896-003-03	100 in 1 BAG	06/19/2020
5		4.9 g in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 76896-003-04	50 in 1 BAG	06/19/2020
6		4.9 g in 1 POUCH; Type 0: Not a Combination Product
7	NDC: 76896-003-07	100 in 1 BOTTLE	06/19/2020
7		4.9 g in 1 POUCH; Type 0: Not a Combination Product
8	NDC: 76896-003-08	120 in 1 BOTTLE	06/19/2020
8		4.9 g in 1 POUCH; Type 0: Not a Combination Product
9	NDC: 76896-003-09	1000 in 1 BOTTLE	06/19/2020
9		4.9 g in 1 POUCH; Type 0: Not a Combination Product
10	NDC: 76896-003-10	80 in 1 BAG	06/19/2020
10		4.9 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/19/2020

Labeler - ZHEJIANG BINGER NONWOVEN CO., LTD. (529311763)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG BINGER NONWOVEN CO., LTD.		529311763	manufacture(76896-003)