FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
WAG LABS, INC.
Effective date
2017-11-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:52

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:
Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antibacterial

WARNINGS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more that 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

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

For children under 6 use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanoamine

OTHER SAFETY INFORMATION

Other Information

Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics

INDICATIONS & USAGE SECTION

Uses

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71828-001-012023-01-30C16284748780-1f386c64a-4092-0266-e053-dadaa90a7c1a5ce721cf-47b8-3cac-e053-2a91aa0adf13

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71828-001-01Hand Sanitizer30 mL in 1 BOTTLE, PLASTICGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71828-001HAND SANITIZER (ETHYL ALCOHOL) GEL [WAG LABS, INC.]1Legacy NDC, 1 package rows20171101_5ce721cf-47b8-3cac-e053-2a91aa0adf13.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71828-00171828-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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

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
5ce721cf-47b9-3cac-e053-2a91aa0adf135ce721cf-47b8-3cac-e053-2a91aa0adf132017-11-01WarningsExact identifier
spl id: 5ce721cf-47b9-3cac-e053-2a91aa0adf13
spl set id: 5ce721cf-47b8-3cac-e053-2a91aa0adf13

Reported adverse events (FAERS/openFDA)#

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