FDA.reportPublic FDA data

GLOBAL CARE GOLD ANTIBACTERIAL HAND

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2024-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:39:06

Label at a glance#

ProductGLOBAL CARE GOLD ANTIBACTERIAL HAND
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

for hand washing to decrease bacteria on the skin.

Dosage and administration

wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly.

Label contents#

Full prescribing information#

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 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

  • wet hands as needed
  • lather vigorously for at least 15 seconds
  • rinse and dry thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Sodium Cocoamphoacetate, PEG-150 Distearate, Fragrance, PEG-40 Hydrogenated Castor Oil, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No. 5, FD&C Red No.40

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76176-159-01GLOBAL CARE GOLD ANTIBACTERIAL HAND400 mL in 1 BOTTLE, PUMPLIQUID4001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76176-159GLOBAL CARE GOLD ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LIQUID [NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.]1Current NDC, 1 package rows20241127_27ba0f30-e066-f240-e063-6394a90ae7cb.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-15976176-159-01

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
NameUNIIKind
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
WATER059QF0KO0RIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 40WZB9127XOAIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT

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
GLOBAL CARE GOLD ANTIBACTERIAL HANDBENZALKONIUM CHLORIDENINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.27ba0f30-e066-f240-e063-6394a90ae7cb2024-01-01WarningsExact identifier
ndc (package): 76176-159-01
ndc (product): 76176-159
ndc11 (package): 76176015901
spl id: 27ba126e-a262-f802-e063-6394a90a25eb
spl set id: 27ba0f30-e066-f240-e063-6394a90ae7cb

Reported adverse events (FAERS/openFDA)#

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