3M Hand Sanitizer

Manufacturer
3M Company
Effective date
2020-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:41

Label at a glance#

Product3M Hand Sanitizer
Active ingredientAlcohol
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on the 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

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Caprylic/Capric Triglyceride, Aminomethyl Propanol

Questions?

OTC - QUESTIONS SECTION

1-800-537-2191

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth • in case of contact with eyes, rinse thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

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 Poison Control Center right away.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3M

Hand

Sanitizer

Kills 99.99%

of germs

With Moisturizers

to leave hands

feeling smooth

2 FL OZ (59 mL)

34-8726-1856-5

Principal Display Panel
Principal Display Panel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17518-02017518-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
2484afec-783b-430b-b606-cb2027dcdb89d2572569-7e05-49f6-88e0-73bbc8d8a96e2022-07-15WarningsExact identifier
spl set id: d2572569-7e05-49f6-88e0-73bbc8d8a96e

Reported adverse events (FAERS/openFDA)#

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