Hand Sanitizer

Manufacturer
Henan Deyuanxiang Biological Technology Co., Ltd.
Effective date
2020-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:27

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

●wet hands thoroughly with product and rub into skin until dry●for children under 6, use only under adult supervision●not recommended for infants.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75.0%

Purpose

OTC - PURPOSE SECTION

Antiseptic

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: hands.
Flammable. Keep away from fire or flame.
When using this product●keep out of eyes. In case of
contact with eyes, flush thoroughly with water●avoid
contact with broken skin●do not inhale or ingest
Stop use and ask a doctor if●iritation and 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

●wet hands thoroughly with product and
rub into skin until dry●for children under 6, use only
under adult supervision●not recommended for infants.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer,Triethanolamine.

SPL UNCLASSIFIED SECTION

Other information

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75468-001-01Hand Sanitizer50 mL in 1 BOTTLEGEL501
75468-001-02Hand Sanitizer100 mL in 1 BOTTLEGEL1001
75468-001-03Hand Sanitizer500 mL in 1 BOTTLEGEL5001
75468-001-04Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75468-001HAND SANITIZER (ETHYL ALCOHOL) GEL [HENAN DEYUANXIANG BIOLOGICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 4 package rows20200423_a3c2f461-4139-2d5b-e053-2a95a90a2c7b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75468-00175468-001-01, 75468-001-02, 75468-001-03, 75468-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a3c2fb94-8164-f420-e053-2995a90ace64a3c2f461-4139-2d5b-e053-2a95a90a2c7b2020-04-20WarningsExact identifier
spl id: a3c2fb94-8164-f420-e053-2995a90ace64
spl set id: a3c2f461-4139-2d5b-e053-2a95a90a2c7b

Reported adverse events (FAERS/openFDA)#

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