Hand Sanitizer

Manufacturer
Yiwu Jiefei Daily Chemicals Co.,Ltd.
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:04:38

Label at a glance#

ProductHand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Directions: Wet hands thoroughly and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 62% v/v. Purpose: Antimicarobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Kills 99.9% of germs on the skin.

Warnings

WARNINGS SECTION

Warnings: For extermnal use only. Flammable.
Keep away from heat and flame.
When using this product: avoid contact with face, eyes,
and broken skin. In case of eye contact, flush with plenty
of water and seek medical advice. Stop use and ask a
doctor if rritation or redness develops.
Keep out of reach of children. .
If swallowed, get medical help or contact a
Poison Control Center.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly and rub into skin until
dry. Children under 6 years of age should be supervised
by an adult when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Glycerine,
Carbomer, VE, Flavor

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020119isopropyl alcohol 62 % Topical GelPSN2
1020119isopropyl alcohol 0.62 ML/ML Topical GelSCD2
1020119isopropyl alcohol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73946-001-01Hand Sanitizer2 in 1 CONTAINERGEL22
73946-001-01Hand Sanitizer24 in 1 CARTONGEL242
73946-001-02Hand Sanitizer96 in 1 CARTONGEL962
73946-001-02Hand Sanitizer24 in 1 BOXGEL242
73946-001-03Hand Sanitizer24 in 1 BOXGEL242
73946-001-03Hand Sanitizer96 in 1 CARTONGEL962
73946-001-04Hand Sanitizer24 in 1 CARTONGEL242
73946-001-04Hand Sanitizer2 in 1 CONTAINERGEL22
73946-001-05Hand Sanitizer237 mL in 1 BOTTLEGEL2372
73946-001-05Hand Sanitizer24 in 1 CARTONGEL242
73946-001-06Hand Sanitizer24 in 1 CARTONGEL242
73946-001-06Hand Sanitizer500 mL in 1 BOTTLEGEL5002
73946-001-07Hand Sanitizer72 in 1 CARTONGEL722
73946-001-07Hand Sanitizer100 mL in 1 BOTTLEGEL1002
73946-001-08Hand Sanitizer1000 mL in 1 BOTTLEGEL10002
73946-001-08Hand Sanitizer12 in 1 CARTONGEL122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73946-001HAND SANITIZER (ETHYL ALCOHOL) GEL [YIWU JIEFEI DAILY CHEMICALS CO.,LTD.]2Legacy NDC, 16 package rows20200401_a22fccbb-c047-86ce-e053-2995a90ab5bb.zip

Products#

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

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

NDC Codes#

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
a2309eb3-1472-3995-e053-2995a90ae0bba22fccbb-c047-86ce-e053-2995a90ab5bb2020-03-31WarningsExact identifier
spl id: a2309eb3-1472-3995-e053-2995a90ae0bb
spl set id: a22fccbb-c047-86ce-e053-2995a90ab5bb

Reported adverse events (FAERS/openFDA)#

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