FDA.reportPublic FDA data

Unscented

Manufacturer
Sante Manufacturing Inc
Effective date
2017-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:14

Label at a glance#

ProductUnscented Refill
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients - ethyl Alcohol 70%

OTC - PURPOSE SECTION

Purpose - Antiseptic

INDICATIONS & USAGE SECTION

Use hand sanitizer to help reduce disease causing bacteria on the skin

WARNINGS SECTION

Flammable

OTHER SAFETY INFORMATION

Keep Away from fire or flame

GENERAL PRECAUTIONS SECTION

For external use only

OTC - WHEN USING SECTION

Avoid Contact with eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally to hands and rub thoroughly until dry
  • Supervise children in the use of this product

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unscented RefillUnscented RefillSpaSoap

Extra Strength with Moisturizers & Vitamin E

Hand Sanitizer

Kills 99% of Germs

Unscented

Refill

32oz / 947ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71020-014-322020-01-31C16284748780-19d75b9d1-04f2-f424-e053-dadaa90a57ce4a702a6e-08a8-55f9-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71020-014-32UnscentedRefill947 mL in 1 BOTTLE, PLASTICLIQUID9471

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71020-014UNSCENTED REFILL (HAND SANITIZER) LIQUID [SANTE MANUFACTURING INC]1Legacy NDC, 1 package rows20170311_4a702a6e-08a8-55f9-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71020-01471020-014-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
4a702a6e-08a9-55f9-e054-00144ff88e884a702a6e-08a8-55f9-e054-00144ff88e882017-03-11WarningsExact identifier
spl id: 4a702a6e-08a9-55f9-e054-00144ff88e88
spl set id: 4a702a6e-08a8-55f9-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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