FDA.reportPublic FDA data

Antibacterial Hand Sanitizer

Manufacturer
Hit Promotional Products, Inc.
Effective date
2023-01-01
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:32:31

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

For Hand Sanitizing

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under the age of 6 use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only – hands.
Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under the age of 6 use only under adult supervision.
  • Not recommended for infants.

Other Information

OTHER SAFETY INFORMATION

  • Do not store above 105oF.
  • May discolor some fabric.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Fragrance, Aloe vera Gel.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Hand Sanitizer
Net contents 1 Gallon (128 fl. oz.)
#94989 Hit® ASI-61125
Made in the USA
Hit Promotional Products Inc. Largo, FL
Lot: 000000 Exp. Date: 00/00/00

94989 Label94989 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70204-509-012023-04-26C16284748780-1f386c649-e470-0266-e053-dadaa90a7c1a2dda666c-24fb-45c7-a29b-ab299efa33f3
70204-509-022023-04-26C16284748780-1f386c649-e470-0266-e053-dadaa90a7c1a2dda666c-24fb-45c7-a29b-ab299efa33f3

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
70204-50970204-509-01, 70204-509-02, 70204-509-03
65133-120

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
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
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
efd70d99-7b25-53f8-e053-2a95a90aa5cf2dda666c-24fb-45c7-a29b-ab299efa33f32023-01-01WarningsExact identifier
spl id: efd70d99-7b25-53f8-e053-2a95a90aa5cf
spl set id: 2dda666c-24fb-45c7-a29b-ab299efa33f3

Reported adverse events (FAERS/openFDA)#

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