FDA.reportPublic FDA data

Alcohol

Manufacturer
Relief-Mart, Inc | Generitech Corporation
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:47

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

AlcoholAlcohol

OTC - ASK DOCTOR SECTION

Ask a DoctorAsk a Doctor

Use

INDICATIONS & USAGE SECTION

Use - For hand-washing to decrease bacteria on the skin, only when water is not available.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Stop Use

OTC - STOP USE SECTION

irritation and redness develop

Warning Section

WARNINGS SECTION

Flammable, keep away from fire and flames. For external use only.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin, carbopol, water, propylene glycol, fragrance

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041498ethanol 80 % Topical GelPSN2
1041498ethanol 0.8 ML/ML Topical GelSCD2
1041498ethanol 80 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67285-104-022022-07-29C16284748780-1e4f33bdf-a865-d8a0-e053-dadaa90a6e4eHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67285-104-02Alcohol59 mL in 1 BOTTLE, DISPENSINGGEL592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67285-104ALCOHOL (HAND SAFE HAND SANITIZER GEL) GEL [RELIEF-MART, INC]2Legacy NDC, 1 package rows20220114_a977c3b5-144d-b538-e053-2a95a90ad051.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67285-10467285-104-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT

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
d57e2267-c7e8-7ece-e053-2995a90a36a1a977c3b5-144d-b538-e053-2a95a90ad0512022-01-13WarningsExact identifier
spl id: d57e2267-c7e8-7ece-e053-2995a90a36a1
spl set id: a977c3b5-144d-b538-e053-2a95a90ad051

Reported adverse events (FAERS/openFDA)#

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