Hand Sanitizer

Manufacturer
Yiwu Jiefei Daily Chemicals Co.,Ltd.
Effective date
2020-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:12

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

*spray hands thoroughly with product and allow to dry without wiping●for children under 6, use only under adult supervision ●not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

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 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 irritation and redness develop and
persist 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

*spray hands thoroughly with product and allow to dry
without wiping●for children under 6, use only under adult supervision
●not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Carbomer,Glycerine.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1111

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73946-004-01Hand Sanitizer4 in 1 CARTONGEL41
73946-004-01Hand Sanitizer24 in 1 BOXGEL241
73946-004-02Hand Sanitizer6 in 1 CARTONGEL61
73946-004-02Hand Sanitizer24 in 1 BOXGEL241
73946-004-03Hand Sanitizer6 in 1 CARTONGEL61
73946-004-03Hand Sanitizer24 in 1 BOXGEL241
73946-004-04Hand Sanitizer6 in 1 CARTONGEL61
73946-004-04Hand Sanitizer24 in 1 BOXGEL241
73946-004-05Hand Sanitizer48 in 1 CARTONGEL481
73946-004-05Hand Sanitizer100 mL in 1 BOTTLEGEL1001
73946-004-06Hand Sanitizer24 in 1 CARTONGEL241
73946-004-06Hand Sanitizer237 mL in 1 BOTTLEGEL2371
73946-004-07Hand Sanitizer250 mL in 1 BOTTLEGEL2501
73946-004-07Hand Sanitizer24 in 1 CARTONGEL241
73946-004-08Hand Sanitizer500 mL in 1 BOTTLEGEL5001
73946-004-08Hand Sanitizer16 in 1 CARTONGEL161

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73946-004HAND SANITIZER (ETHYL ALCOHOL) GEL [YIWU JIEFEI DAILY CHEMICALS CO.,LTD.]1Legacy NDC, 16 package rows20200611_a7c65339-92bc-a491-e053-2995a90a624a.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.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
WATER059QF0KO0RIACT
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
a7c63616-7115-1931-e053-2a95a90ab924a7c65339-92bc-a491-e053-2995a90a624a2020-06-10WarningsExact identifier
spl id: a7c63616-7115-1931-e053-2a95a90ab924
spl set id: a7c65339-92bc-a491-e053-2995a90a624a

Reported adverse events (FAERS/openFDA)#

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