Hand Sanitizer

Manufacturer
St. George Spirits, Inc.
Effective date
2021-01-29
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 22:54:20

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure16 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, carbomer, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel 748181-651-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74181-651-01 74181651017418165101

74181-651-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74181-651-02 236.59mL236.59mL

74181-651-03 3784.4mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74181-651-0374181-651-03

748181-651-04

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74181-651-04 18,927mL 74181-651-0474181-651-04

74181-651-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74181-651-05 208198mL 74181-651-0574181-651-05

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74181-65174181-651-03, 74181-651-02, 74181-651-01, 74181-651-04, 74181-651-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
ba144c68-ddef-08ba-e053-2995a90a8307a22dc77b-a085-2591-e053-2a95a90ab5d22021-01-29WarningsExact identifier
spl id: ba144c68-ddef-08ba-e053-2995a90a8307
spl set id: a22dc77b-a085-2591-e053-2a95a90ab5d2

Reported adverse events (FAERS/openFDA)#

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