Zogics Antibacterial wipes

Manufacturer
Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:47

Label at a glance#

ProductZogics Antibacterial wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

●Open top of bag by tearing at notch across to access resealable zipper. ●Pull zipper apart to create a 2”opening at center. ●Place bag of wet wipes upright into the dispenser. ●Pull wipes from center and guide accordingly through the dispensing hole. ●Simply wipe surface to be disinfected and allow surface to air dry 4 minutes before use. Other information ●Lot No. Manufacture date and Expiration date can be foun...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

●For hand sanitizing to decrease bacteria on the skin.
●Apply topically to the skin to help prevent cross contamination.
●Not Recommended for repeated use.
●Dries in seconds.

Warning

WARNINGS SECTION

Warnings■flammable, keep away from fire and flame■do not use in
or around the eyes■stop use and ask a doctor if too much skin irritation
develops or sensitivity develops or increases■keep out of reach of
children. If swallowed, contact medical help or call Poison Control
immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children. If swallowed, contact medical help or call Poison Control immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

●Open top of bag by tearing at notch across to access
resealable zipper.
●Pull zipper apart to create a 2”opening at center.
●Place bag of wet wipes upright into the dispenser.
●Pull wipes from center and guide accordingly through
the dispensing hole.
●Simply wipe surface to be disinfected and allow
surface to air dry 4 minutes before use.
Other information
●Lot No. Manufacture date and Expiration date can be
found on package.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, DMDM Hydantoin, Ethylparaben,
Methylparaben, Polysorbate 20, Fragrance, Disodium
EDTA, Sodium Citrate, Cetylpyridinium Chloride.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75109-51175109-511-01, 75109-511-02, 75109-511-03, 75109-511-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
da8a8beb-b404-0c03-e053-2995a90a9b45a9f73648-5d8b-56a8-e053-2a95a90a15db2022-03-18WarningsExact identifier
spl set id: a9f73648-5d8b-56a8-e053-2a95a90a15db

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.