ANTIBACTERIAL HAND SANITIZER- benzalkonium chloride gel

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

Purpose

Antibacterial

Use

for hand washing to decrease bacteria on skin

WARNINGS

For External use only-hands.

Flammmable.Keep away from head and falme.

When using this produt.keep out of eyes.in case of contact with eyes.Flush throughtly with water.

Avoid contact with broken skin.Do not inhale or ingest.

Stop use and ask a doctor.if skin irritation develops.

keep out of reach of children

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

Directions

Wet hands throughly with product and allow to dry without wiping.For children under 6 use only under adult Supervision.Not recommended for infants.

Inactive ingredients

Cocoamidopropy betaine,sodium alcohol ehtersulphate,fragrance,glycerin,aloe barbadensis flower extract,methylisothiazolinone,water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51414-800
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA FLOWER (UNII: 575DY8C1ER)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51414-800-01	5 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
2	NDC: 51414-800-02	8 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
3	NDC: 51414-800-03	10 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
4	NDC: 51414-800-04	15 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
5	NDC: 51414-800-05	20 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
6	NDC: 51414-800-06	30 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
7	NDC: 51414-800-07	40 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
8	NDC: 51414-800-08	50 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
9	NDC: 51414-800-09	60 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
10	NDC: 51414-800-10	90 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
11	NDC: 51414-800-11	120 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
12	NDC: 51414-800-12	150 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
13	NDC: 51414-800-13	180 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
14	NDC: 51414-800-14	210 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
15	NDC: 51414-800-15	240 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
16	NDC: 51414-800-16	270 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
17	NDC: 51414-800-17	300 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
18	NDC: 51414-800-18	330 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
19	NDC: 51414-800-19	360 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
20	NDC: 51414-800-20	390 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
21	NDC: 51414-800-21	420 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
22	NDC: 51414-800-22	450 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2016
23	NDC: 51414-800-23	480 g in 1 BOTTLE; Type 0: Not a Combination Product	11/16/2016
24	NDC: 51414-800-24	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(51414-800)