FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Xiangtan Ruiqi Import and Export Co Ltd
Effective date
2025-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:38:41

Label at a glance#

ProductHAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

●Place enough product in your palm to thoroughly cover your hands. ●Rub hands together briskly until dry. ●Children under 6 should be supervised by an adult when using this product.

Storage and handling

No

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.06%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

●To decrease bacteria on the skin.
●Recommended or repeated use.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use in the ears, eyes, or mouth.

OTC - WHEN USING SECTION

When using this product, avoid contact with
eyes. In case of eye contact, flush eyes with
water.

OTC - STOP USE SECTION

Stop using the product if it disagrees with you.

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 in your palm to thoroughly cover your hands.
●Rub hands together briskly until dry.
●Children under 6 should be supervised by an adult when using this product.

Other information

STORAGE AND HANDLING SECTION

No

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Benzalkonium Chloride, Glycerin, Fragrance, Aloe Vera Extract,
Camellia OleiferaSeed Oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85733-001HAND SANITIZER LIQUID [XIANGTAN RUIQI IMPORT AND EXPORT CO LTD]1Unmatched20250528_35c4f007-c952-8e51-e063-6294a90aea17.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85733-00185733-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
FRAGRANCE 135765EM498GW35IACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CAMELLIA OLEIFERA SEED59ED29FM2JIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
48c9cb90-15b7-3142-e063-6394a90a5b6235c4f007-c952-8e51-e063-6294a90aea172026-01-19WarningsExact identifier
spl set id: 35c4f007-c952-8e51-e063-6294a90aea17

Reported adverse events (FAERS/openFDA)#

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