MEDISIDE-HAND ANTISEPTIC TISSUE- benzalkonium chloride liquid 
YOU HAN GREENTECH

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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78583-701

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

79893-402-01

79893-402-02

79893-402-03

MEDISIDE-HAND ANTISEPTIC TISSUE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78583-701
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
ORANGE OIL (UNII: AKN3KSD11B)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78583-701-0166 g in 1 POUCH; Type 0: Not a Combination Product06/04/2021
2NDC:78583-701-02132 g in 1 POUCH; Type 0: Not a Combination Product06/04/2021
3NDC:78583-701-03198 g in 1 POUCH; Type 0: Not a Combination Product06/04/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/04/2021
Labeler - YOU HAN GREENTECH (688304505)
Registrant - YOU HAN GREENTECH (688304505)
Establishment
NameAddressID/FEIBusiness Operations
YOU HAN GREENTECH688304505manufacture(78583-701)

Revised: 7/2022
Document Id: e308af8e-65fa-f986-e053-2995a90a74d2
Set id: e309c797-8009-82ae-e053-2a95a90a4ffd
Version: 4
Effective Time: 20220705
 
YOU HAN GREENTECH