ANTIBACTERIAL MOISTURIZING HAND WIPES- benzalkonium chloride liquid

Antibacterial Moisturizing Hand Wipes by

Drug Labeling and Warnings

Antibacterial Moisturizing Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Yinjing Medical Technology (Shanghai) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Antibacterial Moisturizing Hand Wipes

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

Decrease bacteria on the skin

Warnings

For external use only

Do not use

if you are allergic to any of the ingredients.

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs and continues for more than 72 hours.

Keep out of reach of children

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

Directions

Lift package label to open and remove wipe.
Wipe hands thoroughly. Allow to dry.
Discard wipe in trash. Do not flush.
Re-seal package after each use to avoid evaporation.
For children under 2 year, Consult a physician before use.

Inactive ingredients

Water, Glycerin, Propylene Glycol, Polysorbate-20, Phenoxyethanol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Diazolidinyl Urea, Decyl Glucoside, Disodium EDTA, Sodium Citrate, Fragrance.

IN IN

Shanghai Yinjing Medical Supplies Co.,Ltd.
Add: No.586YuanXi Rd, Nanhui Industry Park,
Pudong new area,Shanghai.China.
Tel:+86-(21)68016511 Fax:+86-(21)68016736
http://www.yinjing.cn E-mail:zhl@yinjing.cn

PRINCIPAL DISPLAY PANEL

IN IN  NDC:  Antibacterial Moisturizing Hand Wipes  15 wipes 5.12 x 7.87 in (13cm x 20 cm)  Kills 99.9% of Germs   Contains Moisturizers, Vitamin E and Aloe

Antibacterial Moisturizing Hand Wipes 15 Wipes (

44019-000-00)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL MOISTURIZING HAND WIPES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44019-000
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44019-000-00	15 in 1 BAG	08/03/2016
1		2.7 g in 1 PATCH; 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	part333E	07/08/2013

Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)

Registrant - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)