GLOBAL CARE GOLD ANTIBACTERIAL HAND

Manufacturer: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date: 2020-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:25:22

Label at a glance#

ProductGLOBAL CARE GOLD ANTIBACTERIAL HAND

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

for hand washing to decrease bacteria on the skin.

Dosage and administration

pump into hands lather vigorously for at least 15 seconds rinse and dry thoroughly

Label contents#

Full prescribing information#

Drug Facts Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13 percent

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

pump into hands
lather vigorously for at least 15 seconds
rinse and dry thoroughly

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropye Betaine, PEG-6000 Distearate, Sodium Cocoamphoacetate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No.5, D&C Red No.33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

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

GLOBAL CARE GOLD ANTIBACTERIAL HAND
BENZALKONIUM CHLORIDE
WATER
COCAMIDOPROPYL BETAINE
SODIUM COCOAMPHOACETATE
IODOPROPYNYL BUTYLCARBAMATE
CITRIC ACID MONOHYDRATE
METHYLISOTHIAZOLINONE
BENZALKONIUM
D&C RED NO. 33
FD&C YELLOW NO. 5
PEG-150 DISTEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76176-098	76176-098-01

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
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
SODIUM COCOAMPHOACETATE	W7Q5E87674	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
D&C RED NO. 33	9DBA0SBB0L	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
PEG-150 DISTEARATE	6F36Q0I0AC	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
a844d3fe-e03b-b5fb-e053-2a95a90ab0a5			a844d3fe-e03a-b5fb-e053-2a95a90ab0a5	2020-06-01	Warnings	Exact identifier spl id: a844d3fe-e03b-b5fb-e053-2a95a90ab0a5 spl set id: a844d3fe-e03a-b5fb-e053-2a95a90ab0a5

Reported adverse events (FAERS/openFDA)#

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