Hand Sanitizer

Manufacturer
Hub Pen (HPG Brands) | HUB PEN COMPANY, INC. | BEACON PROMOTIONS, INC. | BEST PROMOTIONS U.S.A., LLC | Handstands Promo
Effective date
2022-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:56

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand Sanitizer to help decrease bacteria on the skin.

Dosage and administration

Remove wipe from pouch, throughly wash hands and arms with wipe and discard wipe when finished. Do not flush wipe. Children under 6 years should be supervised when using this product.

Label contents#

Full prescribing information#

Ethyl Alcohol 75%

OTC - ACTIVE INGREDIENT SECTION

activeactive

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin.

usesuses

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

Fr external use only.

warnwarn

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, rinse with water.

whenwhen

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

stopstop

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly and contact Poison Control.

keepkeep

Directions

DOSAGE & ADMINISTRATION SECTION

Remove wipe from pouch, throughly wash hands and arms with wipe and discard wipe when finished. Do not flush wipe.

Children under 6 years should be supervised when using this product.

dirdir

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

waterwater

Purpose

OTC - PURPOSE SECTION

Antiseptic

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDPHand Sanitizer Wipes

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77988-00177988-001-10, 77988-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
eb68926b-a85d-d993-e053-2a95a90ad318a7ad9452-c4c3-59a8-e053-2995a90a2fcc2022-10-19WarningsExact identifier
spl set id: a7ad9452-c4c3-59a8-e053-2995a90a2fcc

Reported adverse events (FAERS/openFDA)#

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