FDA.reportPublic FDA data

HAND WASH

Manufacturer
ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
Effective date
2024-04-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:05:08

Label at a glance#

ProductHAND WASH
Active ingredientBENZALKONIUM CHLORIDE, DIDECYLDIMONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Do not store above 105°F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Didecyldimonium Chloride 0.2%
Benzalkoniumchloride 0.26%

Purpose

OTC - PURPOSE SECTION

Hand wish

Use

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable.
  • Keep away from fire or flame.

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin.
  • do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor

  • if airritation or redness develops.
  • condition persists for more than 72 hours.

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

  • Place enough product on hands to cover all surfaces Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 105°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250ML NDC:73905-035-01 500ml label500ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73905-035-012024-04-18C16284748780-1f386c649-d6c5-0266-e053-dadaa90a7c1acfe43205-ebdb-6c7e-e053-2995a90a13c8
73905-035-012023-01-30C16284748780-1f386c649-d6c5-0266-e053-dadaa90a7c1acfe43205-ebdb-6c7e-e053-2995a90a13c8

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73905-03573905-035-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BACTIB
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
165eec81-773e-46c8-e063-6294a90ab8f2cfe43205-ebdb-6c7e-e053-2995a90a13c82024-04-18WarningsExact identifier
spl id: 165eec81-773e-46c8-e063-6294a90ab8f2
spl set id: cfe43205-ebdb-6c7e-e053-2995a90a13c8

Reported adverse events (FAERS/openFDA)#

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