Antibacterial Hand Sanitizer

Manufacturer
Hit Promotional Products, Inc.
Effective date
2020-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:30:51

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

• For Hand Sanitizing

Dosage and administration

• Wet hands thoroughly with product and allow to dry without wiping. • For children under 6 age 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.

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 6 age use only under adult supervision.
  • Not recommended for infants.

Other Information

OTHER SAFETY INFORMATION

  • Do not store above 105F.
  • May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water. Blue 1 (CI 42090), Red 33 (CI 17200)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Hand Sanitizer
.5 fl. oz.

0.5oz #9067
Hit® ASI-61125
HIT Promotional Product Inc.
Largo, FL.
Made in China

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Label

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70204-50570204-505-01, 70204-505-02

Ingredients#

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

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

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
4b7e5d39-a147-4cd8-bd2d-4a1c76fd2ec94b7e5d39-a147-4cd8-bd2d-4a1c76fd2ec92020-05-11WarningsExact identifier
spl id: 4b7e5d39-a147-4cd8-bd2d-4a1c76fd2ec9
spl set id: 4b7e5d39-a147-4cd8-bd2d-4a1c76fd2ec9

Reported adverse events (FAERS/openFDA)#

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