FDA.reportPublic FDA data

GOLDESSENCE Antibacterial Wet Wipes

Manufacturer
Zhejiang Youbeisi Daily Chemical Technology Co., Ltd.
Effective date
2020-07-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:35

Label at a glance#

ProductGOLDESSENCE Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Wipe the surface of the skin and let it air dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

GOLDESSENCE Antibacterial Wet Wipes

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.0052mg/pcs. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, GOLDESSENCE Antibacterial Wet Wipes

Use

INDICATIONS & USAGE SECTION

GOLDESSENCE Antibacterial Wet Wipes to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Wipe the surface of the skin and let it air dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Chlorphenesin
Fragrance
Phenoxyethanol
DIDECYLDIMONIUM CHLORIDE
Propylene Glycol
Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2211

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79387-104-012021-07-23C16284748780-1c7ccaba7-26ca-fd44-e053-dadaa90aa01bGOLDESSENCE Antibacterial Wet Wipes
79387-104-022021-07-23C16284748780-1c7ccaba7-26ca-fd44-e053-dadaa90aa01bGOLDESSENCE Antibacterial Wet Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79387-104-01GOLDESSENCE Antibacterial Wet Wipes75 in 1 CANISTERCLOTH751
79387-104-02GOLDESSENCE Antibacterial Wet Wipes75 in 1 CANISTERCLOTH751

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79387-104GOLDESSENCE ANTIBACTERIAL WET WIPES (BENZALKONIUM CHLORIDE) CLOTH [ZHEJIANG YOUBEISI DAILY CHEMICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 2 package rows20200725_ab2e75aa-79bd-786a-e053-2995a90a29ef.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79387-10479387-104-01, 79387-104-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CHLORPHENESINI670DAL4SZIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PHENOXYETHANOLHIE492ZZ3TIACT

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
ab2e75aa-79ae-786a-e053-2995a90a29efab2e75aa-79bd-786a-e053-2995a90a29ef2020-07-24WarningsExact identifier
spl id: ab2e75aa-79ae-786a-e053-2995a90a29ef
spl set id: ab2e75aa-79bd-786a-e053-2995a90a29ef

Reported adverse events (FAERS/openFDA)#

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