Antibacterial Hand Wipes

Manufacturer: GoodFibers
Effective date: 2022-01-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:47:26

Label at a glance#

ProductAntibacterial Hand Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Indications and uses

*For hand washing to decrease bacteria on skin without requiring water or rinsing. *Recommended for repeated use

Dosage and administration

*Wet thoroughly hands with wipe and allow to dry without wiping. *Children under six years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium

Chloride 0.125%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

USES

INDICATIONS & USAGE SECTION

*For hand washing to decrease bacteria on skin without requiring water or rinsing.

*Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

When using product

OTC - WHEN USING SECTION

*Do not use in or near eyes.

If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

*If irritation and redness persist for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental indestion, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

*Wet thoroughly hands with wipe and allow to dry without wiping.

*Children under six years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citric Acid, Decyl Glucoside, Fragrtance, Phenoxyethanol, Potassium Sorbate, Tetrasodium EDTA, Water.

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelMEDIC THERAPEUTICS

ANTIBACTERIAL

HAND WIPES

___________________

KILLS 99.9% OF GERMS

Sanitize on the Go

Active Ingredient -

Benzalkonium Chloride (0.125%)

7 x 5.1in (18 x 13 cm)

20 CT

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2276303	benzalkonium Cl 0.125 % Medicated Pad	PSN	2
2276303	benzalkonium chloride 1.25 MG/ML Medicated Pad	SCD	2
2276303	benzalkonium chloride 0.125 % Medicated Wipe	SY	2
2276303	benzalkonium chloride 0.125 % Topical Cloth	SY	2
2276303	benzalkonium chloride 0.125 % Topical Swab	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77070-702-20	2024-01-30	C162847	48780-1	1030e365-6cf6-111a-e063-dadaa90a10e2	Antibacterial Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77070-702-20	Antibacterial Hand Wipes	1 g in 1 POUCH	CLOTH	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77070-702	ANTIBACTERIAL HAND WIPES CLOTH [GOODFIBERS]	2	Legacy NDC, 1 package rows	20220123_aa99e7cf-7b11-0e7b-e053-2995a90a98bc.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Antibacterial Hand Wipes
ALOE VERA LEAF
BENZALKONIUM CHLORIDE
BENZALKONIUM
PHENOXYETHANOL
WATER
ANHYDROUS CITRIC ACID
DECYL GLUCOSIDE
EDETATE SODIUM
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77070-702	77070-702-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	IACT
WATER	059QF0KO0R	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
EDETATE SODIUM	MP1J8420LU	IACT
POTASSIUM SORBATE	1VPU26JZZ4	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
d6269116-e51f-eb4e-e053-2a95a90ae951			aa99e7cf-7b11-0e7b-e053-2995a90a98bc	2022-01-22	Warnings	Exact identifier spl id: d6269116-e51f-eb4e-e053-2a95a90ae951 spl set id: aa99e7cf-7b11-0e7b-e053-2995a90a98bc

Reported adverse events (FAERS/openFDA)#

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