ANTIBACTERIAL HAND SANITIZER- benzalkonium chloride spray

antibacterial hand sanitizer by

Drug Labeling and Warnings

antibacterial hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Yuyao Jessie Commodity Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium chloride 0.4%

Purpose

Antibacterial

Use

for hand washing to decrease bacteria on skin

WARNINGS

For External use only-hands.

When using this produt.avoid contact with eyes.In case of eye contact ,flush eyes with water.

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

keep out of reach of children if swallowed,get medical help to contact a poison control center reght away

keep out of reach of children unless under adult supervision .if seallowed ,get medical help or contact a Poison Control Center immediately.

Directions

Pump a small amout into palm

rub thoroughly over all surfaces of both hands,rub hands to gether birskly until dry.

Inactive ingredients

Deionizer Water, Glycerin, Silicone oil, Aloe Barbadensis Leaf Extrac, Propylene glycol, Kathon, EDTA-2NA, Tocopherol Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51414-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA FLOWER (UNII: 575DY8C1ER)
EDETIC ACID (UNII: 9G34HU7RV0)
SILICON (UNII: Z4152N8IUI)
PROPYLENE GLYCOL BEHENATE (UNII: Z101D9Y62T)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51414-103-01	5 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
2	NDC: 51414-103-02	8 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
3	NDC: 51414-103-03	10 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
4	NDC: 51414-103-04	15 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
5	NDC: 51414-103-05	20 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
6	NDC: 51414-103-06	30 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
7	NDC: 51414-103-07	40 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
8	NDC: 51414-103-08	50 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
9	NDC: 51414-103-09	60 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
10	NDC: 51414-103-10	90 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
11	NDC: 51414-103-11	120 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
12	NDC: 51414-103-12	150 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
13	NDC: 51414-103-13	180 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
14	NDC: 51414-103-14	210 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
15	NDC: 51414-103-15	240 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
16	NDC: 51414-103-16	270 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
17	NDC: 51414-103-17	300 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
18	NDC: 51414-103-18	330 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
19	NDC: 51414-103-19	360 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
20	NDC: 51414-103-20	390 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
21	NDC: 51414-103-21	420 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
22	NDC: 51414-103-22	450 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
23	NDC: 51414-103-23	480 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
24	NDC: 51414-103-24	18.3 g in 1 BOTTLE; Type 0: Not a Combination Product	10/19/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/27/2014

Labeler - Yuyao Jessie Commodity Co.,Ltd. (529892305)

Establishment
Name	Address	ID/FEI	Business Operations
Yuyao Jessie Commodity Co.,Ltd.		529892305	manufacture(51414-103)