FDA.reportPublic FDA data

HNJ Products LLC Hand Sanitizer

Manufacturer
HNJ Products LLC | Guangzhou Danting Bath&Body Care Industry Co. Ltd.
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:43:36

Label at a glance#

ProductHNJ Products LLC Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients (s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s):

INDICATIONS & USAGE SECTION

Hand sanitizer 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

  • On children less than 2 months of age
  • On Open skin wounds

When using this product:

OTC - WHEN USING SECTION

Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor:

OTC - STOP USE SECTION

If irritation or rash occurs. These may be signs of a serious condition.

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

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

Other Information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Alcohol, Pure Water, Triethanolamine, Carbomer, Glycerin, Benzalkonium Chloride, Aloe Vera, VItamin E

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79444-005-002025-01-03C16284748780-1d6a99b39-821f-a426-e053-dadaa90af4c2HNJ Products LLC Hand Sanitizer
79444-005-002022-01-28C16284748780-1d6a99b39-821f-a426-e053-dadaa90af4c2HNJ Products LLC Hand Sanitizer

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
79444-00579444-005-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALCOHOL3K9958V90MACTIB

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
3509d185-5b8f-a8de-e063-6394a90a7f3ad33816b4-5ef4-4bf7-b86e-d5b92d7c50ec2025-05-13WarningsExact identifier
spl set id: d33816b4-5ef4-4bf7-b86e-d5b92d7c50ec

Reported adverse events (FAERS/openFDA)#

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