Drs Clean Hand gel

Manufacturer
EROOM FACTORY Co., Ltd.
Effective date
2020-04-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:03

Label at a glance#

ProductDrs Clean Hand gel
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

Ethanol, Deionized Water, 1,3-Butylene Glycol, Aloe Extract, Carbomer, Glycerine, Triethanolamine, Fragrance, Sodium Hyaluronate

OTC - PURPOSE SECTION

Antimicrobial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75193-0001-12022-01-28C16284748780-1d6a99b39-6f0a-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75193-0001-1Drs Clean Hand gel500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75193-0001DRS CLEAN HAND GEL (ALCOHOL) GEL [EROOM FACTORY CO., LTD.]1Legacy NDC, 1 package rows20200413_a31ef289-6bab-c5f0-e053-2a95a90a0557.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
75193-000175193-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a31f053c-f050-0977-e053-2995a90a4ff0a31ef289-6bab-c5f0-e053-2a95a90a05572020-04-12WarningsExact identifier
spl id: a31f053c-f050-0977-e053-2995a90a4ff0
spl set id: a31ef289-6bab-c5f0-e053-2a95a90a0557

Reported adverse events (FAERS/openFDA)#

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