MEDISIDE-HAND ANTISEPTIC TISSUE: Package Insert and Label Information

MEDISIDE-HAND ANTISEPTIC TISSUE- benzalkonium chloride liquid
C & D Specialty Food Inc

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.

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE

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
(click image for full-size original)

79893-402-02
(click image for full-size original)
79893-402-03
(click image for full-size original)
MEDISIDE-HAND ANTISEPTIC TISSUE
benzalkonium chloride liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:79893-402
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 50 g in 100 g
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
ORANGE OIL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:79893-402-01 66 g in 1 POUCH None
2 NDC:79893-402-02 132 g in 1 POUCH None
3 NDC:79893-402-03 198 g in 1 POUCH None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 06/04/2021
Labeler — C & D Specialty Food Inc (117595485)
Registrant — C & D Specialty Food Inc (117595485)
Establishment
Name Address ID/FEI Operations
Yuhan Green Tech Co. 688304505 manufacture (79893-402)

Revised: 06/2021 C & D Specialty Food Inc

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.