MEDISIDE-HAND ANTISEPTIC TISSUE- benzalkonium chloride liquid

MEDISIDE-HAND ANTISEPTIC TISSUE by

Drug Labeling and Warnings

MEDISIDE-HAND ANTISEPTIC TISSUE by is a Otc medication manufactured, distributed, or labeled by YOU HAN GREENTECH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

ANTIMICROBIAL

Direction

To dispense, peel back front label at tab

Remove towelettes as needed

Reseal pouch by pressing label firmly back into place

Do not use

do not flush

do not use if you are allergic to any of the ingredients

Warnings

for external sue only.

sotre away from direct sunlight or high temperature.

use caution near electric appliances to avoid electric shock.

Keep out of reach of children.

Keep out of reach of children.

stop use and ask a doctor.

stop use and ask a doctor if irritationor or rash edvelopes and continues for more than 72 hours.

Use

peel back front label slowy.

use caution near electric appliances to avoid electric shock

ask a doctor

f swallowed, get medical help or contact a Poison control center right away

Other information

7.9 in x 5.9 in (20cm x15cm )

INACTIVE INGREDIEINT

Aqua

Glycerine

Orange Sweet Ext.

Package Label

INGREDIENTS AND APPEARANCE

MEDISIDE-HAND ANTISEPTIC TISSUE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78583-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ORANGE OIL (UNII: AKN3KSD11B)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78583-701-01	66 g in 1 POUCH; Type 0: Not a Combination Product	06/04/2021
2	NDC: 78583-701-02	132 g in 1 POUCH; Type 0: Not a Combination Product	06/04/2021
3	NDC: 78583-701-03	198 g in 1 POUCH; Type 0: Not a Combination Product	06/04/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/04/2021

Labeler - YOU HAN GREENTECH (688304505)

Registrant - YOU HAN GREENTECH (688304505)

Establishment
Name	Address	ID/FEI	Business Operations
YOU HAN GREENTECH		688304505	manufacture(78583-701)