FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Inkwell Global Marketing Corp.
Effective date
2020-05-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:27

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other Information Store below 110 F.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Ethyl Alcohol 75%

OTC - PURPOSE SECTION

Purpose
Antibacterial

INDICATIONS & USAGE SECTION

Uses

Hand sanitizer to reduce bacteria on the skin.

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes.In case of contact, rinse eyes thoroughly with

water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact the Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Place enough product on hand to cover fully
  • Rub hands together until dry
  • Children under 6 years of age should be supervised when using this product.

STORAGE AND HANDLING SECTION

Other Information

Store below 110 F.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Maltodextrin,Glycerin, Propylene Glycol, Acrylates/C1O-30 Alkyl Acrylate crosspolymer, Triethanoamine, Fragrance, Tocopheryl Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77512-002-012025-01-30C16284748780-12cef2736-9b7b-d83d-e063-dadaa90ab31fa5e3fd2e-5bde-110c-e053-2a95a90a59e0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77512-002-01Hand Sanitizer59 mL in 1 BOTTLEGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77512-002HAND SANITIZER (ETHYL ALCOHOL) GEL [INKWELL GLOBAL MARKETING CORP.]1Legacy NDC, 1 package rows20200518_a5e3fd2e-5bde-110c-e053-2a95a90a59e0.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77512-00277512-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
MALTODEXTRIN7CVR7L4A2DIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML · Source PDF

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
a5e3fd2e-5bdf-110c-e053-2a95a90a59e0a5e3fd2e-5bde-110c-e053-2a95a90a59e02020-05-10WarningsExact identifier
spl id: a5e3fd2e-5bdf-110c-e053-2a95a90a59e0
spl set id: a5e3fd2e-5bde-110c-e053-2a95a90a59e0

Reported adverse events (FAERS/openFDA)#

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