Good to Go Antibacterial Hand Wipes

Manufacturer: Navajo Manufacturing Company Inc. | Kangna (Zhejiang) Medical Supplies Co., Ltd.
Effective date: 2022-07-28
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 21:56:10

Label at a glance#

ProductGood to Go Antibacterial Hand Wipes

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

for hand sanitizing to decrease bacteria on the skin recommended for repeated use

Dosage and administration

Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry. Dispose of wipe.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

for hand sanitizing to decrease bacteria on the skin
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of contact, flush eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Take wipe and rub thoroughly over all surfaces of both hands.
Rub hands together briskly to dry.
Dispose of wipe.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Good To Go Antibacterial Hand Wipes

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Good to Go Antibacterial Hand Wipes
benzalkonium chloride
PHENOXYETHANOL
CETYLPYRIDINIUM CHLORIDE
METHYLPARABEN
BENZALKONIUM
WATER
DMDM HYDANTOIN
SODIUM CITRATE
EDETATE DISODIUM ANHYDROUS
ETHYLPARABEN
POLYSORBATE 20

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67751-210	67751-210-50

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
PHENOXYETHANOL	HIE492ZZ3T	IACT
CETYLPYRIDINIUM CHLORIDE	D9OM4SK49P	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
ETHYLPARABEN	14255EXE39	IACT
POLYSORBATE 20	7T1F30V5YH	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
e4e456dc-016c-7514-e053-2a95a90a9169			b98006e0-909e-42c4-e053-2a95a90a55d0	2022-07-28	Warnings	Exact identifier spl id: e4e456dc-016c-7514-e053-2a95a90a9169 spl set id: b98006e0-909e-42c4-e053-2a95a90a55d0

Reported adverse events (FAERS/openFDA)#

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