Antibacterial Wipes

Manufacturer: GULSELI TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Effective date: 2020-06-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:55

Label at a glance#

ProductAntibacterial Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Deionized Water, Tetrasodium EDTA, Sodium Cocoamphoacetate, Glycerin, Dehydroacetic Acid,
Phenoxyethanol, Benzoic Acid, D-Panthenol, Fragrance, Aloe Barbadensis Leaf Juice, Daisy Extrac

OTC - PURPOSE SECTION

Antimicrobial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.2% w/w

OTC - WHEN USING SECTION

do not use in or near the eyes
In case of eye contact, hold eyes open and rinse slowly and gently with water.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - DO NOT USE SECTION

on broken skin
if you are allergic to any of the ingredients.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if, too much skin irritation or sensivity develops or increases.

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years and older: wipe hands and allow to dry without wiping.
children under 2 years: ask a doctor before use.

INDICATIONS & USAGE SECTION

for hand sanitizing to reduce bacteria on the skin.

WARNINGS SECTION

For external use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Full DesignDrug FactsFrontSide

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2360919	benzalkonium Cl 0.2 % Medicated Pad	PSN	1
2360919	benzalkonium chloride 2 MG/ML Medicated Pad	SCD	1
2360919	benzalkonium chloride 0.2 % Medicated Wipe	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79084-001-01	2022-01-28	C162847	48780-1	d6a99b39-7565-a426-e053-dadaa90af4c2	Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79084-001-01	Antibacterial Wipes	100 g in 1 PACKAGE	SWAB	100		1
79084-001-01	Antibacterial Wipes	60 in 1 PACKAGE	SWAB	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79084-001	ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) SWAB [GULSELI TEMIZLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI]	1	Legacy NDC, 2 package rows	20200625_a8628bb6-3111-fb15-e053-2995a90a6ef0.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

Antibacterial Wipes
Benzalkonium Chloride
EDETATE SODIUM
ALOE VERA LEAF
BELLIS PERENNIS FLOWER
PHENOXYETHANOL
DEXPANTHENOL
BENZOIC ACID
GLYCERIN
DEHYDROACETIC ACID
SODIUM COCOAMPHOACETATE
BENZALKONIUM
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79084-001	79084-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
EDETATE SODIUM	MP1J8420LU	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
BELLIS PERENNIS FLOWER	26I94X9A1K	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
DEXPANTHENOL	1O6C93RI7Z	IACT
BENZOIC ACID	8SKN0B0MIM	IACT
GLYCERIN	PDC6A3C0OX	IACT
DEHYDROACETIC ACID	2KAG279R6R	IACT
SODIUM COCOAMPHOACETATE	W7Q5E87674	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a8627b38-93ec-8893-e053-2a95a90acf81			a8628bb6-3111-fb15-e053-2995a90a6ef0	2020-06-18	Warnings	Exact identifier spl id: a8627b38-93ec-8893-e053-2a95a90acf81 spl set id: a8628bb6-3111-fb15-e053-2995a90a6ef0

Reported adverse events (FAERS/openFDA)#

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