FDA.reportPublic FDA data

Hand Sanitizer 70% Gel

Manufacturer
Navajo Manufacturing Company Inc. | Marquis Extraction Technology LLC
Effective date
2021-01-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:56:08

Label at a glance#

ProductHand Sanitizer 70% Gel
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product to cover both hands in the palm, and rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For eternal use only.

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears on the skin.

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 to cover both hands in the palm, and rub hands together until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

  • Store between 59-86°F (15-30°C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylate copolymer, aloe, denatonium benzoate, fragrance, glycerin, water.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-525-5097

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer 70% GelHand Sanitizer 70% Gel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67751-20467751-204-01, 67751-204-02, 67751-204-03, 67751-204-04, 67751-204-05, 67751-204-06, 67751-204-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
LINALOOL, (+)-F4VNO44C09IACT
CUMINYL ACETALDEHYDEWSW8QXE6HGIACT
WATER059QF0KO0RIACT
DENATONIUM BENZOATE ANHYDROUSM5BA6GAF1OIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT

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
e32914fa-8c78-8959-e053-2a95a90a64c0b076c7e3-549e-10c3-e053-2995a90a70c32022-07-06WarningsExact identifier
spl set id: b076c7e3-549e-10c3-e053-2995a90a70c3

Reported adverse events (FAERS/openFDA)#

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