FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
HUB PEN COMPANY, INC. (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
3
Source
legacy-cache
Hydrated at
2026-08-01 22:17:54

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

Place enough product in your palm to throughly cover your hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

Label contents#

Full prescribing information#

Ethyl Alcohol 62%

OTC - ACTIVE INGREDIENT SECTION

back sprayback sprayBack panelBack panel

Antiseptic

OTC - PURPOSE SECTION

back panelback panel

Warnings

WARNINGS SECTION

Flammable. keep away from fire or flame.

For external use only

backback

When Using This Product

OTC - WHEN USING SECTION

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

when usingwhen using

OTC - STOP USE SECTION

Stop use and ask doctor if irritation nad redness develops and persist.

Stop useStop use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

keepkeep

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbomer, fragrance, Glycerin, propilene glycol, Tocopheryl acetate, Triethanolamine, Water

inactiveinactive

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to throughly cover your hands and rub hands together until dry.

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

UsesUses

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin

Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Spray frontSpray frontPDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77988-002-012022-10-19C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b
77988-002-022022-10-19C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b
77988-002-032022-10-19C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b
77988-002-012022-07-29C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b
77988-002-022022-07-29C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b
77988-002-032022-07-29C16284748780-1e4f33bdf-afd7-d8a0-e053-dadaa90a6e4ea618a9ab-0e2f-2458-e053-2995a90a275b

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
77988-00277988-002-02, 77988-002-01, 77988-002-03
77988-00477988-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER 9404Q93RCW27EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT

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
eb6892ce-177b-c67e-e053-2995a90af1a7a618a9ab-0e2f-2458-e053-2995a90a275b2022-10-19WarningsExact identifier
spl set id: a618a9ab-0e2f-2458-e053-2995a90a275b

Reported adverse events (FAERS/openFDA)#

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