FDA.reportPublic FDA data

GLOBAL CARE 7.5OZ ANTIBACTERIAL HAND SWEETPEA ORCHID

Manufacturer
Ningbo Liyuan Daily Chemical Products Co., Ltd | Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2018-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:53:45

Label at a glance#

ProductGLOBAL CARE 7.5OZ ANTIBACTERIAL HAND SWEETPEA ORCHID
Active ingredientCHLOROXYLENOL
Label structure11 sections

Indications and uses

for hand washing to help eliminate bacteria on the skin.

Dosage and administration

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

Storage and handling

store at room temperature.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for hand washing to help eliminate bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product:

OTC - WHEN USING SECTION

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

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

Other Information:

STORAGE AND HANDLING SECTION

store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Sodium Chloride, Fragrance, Glycerin, Citric Acid, PEG-150 Distearate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Red No. 40, FD&C Yellow No. 5.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABELLABEL

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-08376176-083-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
FD&C RED NO. 40WZB9127XOAIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
CHLOROXYLENOL0F32U78V2QACTIB

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
70136107-dff0-9adf-e053-2991aa0a995970136107-dfef-9adf-e053-2991aa0a99592018-05-01WarningsExact identifier
spl id: 70136107-dff0-9adf-e053-2991aa0a9959
spl set id: 70136107-dfef-9adf-e053-2991aa0a9959

Reported adverse events (FAERS/openFDA)#

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