Hand Sanitizer

Manufacturer
NANTONG QINJI HEALTH TECHNOLOGY CO., LTD.
Effective date
2025-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:13

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Squeeze small amount in your palm and briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable.

Keep away from fire or flame.

When using this produce,

OTC - WHEN USING SECTION

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

discontinue use if

OTC - STOP USE SECTION

irritation or redness develops

Keep out 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

Squeeze small amount in your palm and briskly rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide (CI 77499), Iron Oxide (CI 77492), D&C Red No.30.

84641-006-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

84641-006-0184641-006-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84641-006-01Hand Sanitizer15 mL in 1 BOTTLEGEL151

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84641-00684641-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
37c24f24-a3be-b82f-e063-6294a90a696a37c24f18-be70-da9e-e063-6394a90ae73e2025-06-17WarningsExact identifier
spl id: 37c24f24-a3be-b82f-e063-6294a90a696a
spl set id: 37c24f18-be70-da9e-e063-6394a90ae73e

Reported adverse events (FAERS/openFDA)#

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