GLOBAL CARE OCEAN MIST ANTIBACTERIAL FOAMING HAND

Manufacturer: TARGET PRICE, INC | Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date: 2020-04-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:32:10

Label at a glance#

ProductGLOBAL CARE OCEAN MIST ANTIBACTERIAL FOAMING 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), Laureth-9, Sodium Lauroamphoacetate, Glycerin, Citric Acid, Fragrance, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Blue No.1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

GLOBAL CARE OCEAN MIST ANTIBACTERIAL FOAMING HAND
BENZALKONIUM CHLORIDE
WATER
SEC-LAURETH-9
SODIUM LAUROAMPHOACETATE
IODOPROPYNYL BUTYLCARBAMATE
CITRIC ACID MONOHYDRATE
METHYLISOTHIAZOLINONE
GLYCERIN
BENZALKONIUM
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72146-014	72146-014-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SEC-LAURETH-9	441JX1IO3Z	IACT
SODIUM LAUROAMPHOACETATE	SLK428451L	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
FD&C BLUE NO. 1	H3R47K3TBD	IACT

Source Document#

Source XML · Source PDF

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
a52e9bf7-b9e6-280f-e053-2a95a90a7aa8			a52e9bf7-b9e5-280f-e053-2a95a90a7aa8	2020-04-01	Warnings	Exact identifier spl id: a52e9bf7-b9e6-280f-e053-2a95a90a7aa8 spl set id: a52e9bf7-b9e5-280f-e053-2a95a90a7aa8

Reported adverse events (FAERS/openFDA)#

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