Hand Sanitizer

Manufacturer
Elevation Gourmet, Inc.
Effective date
2020-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:21

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure16 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient(s)

Alcohol 80% v/v

OTC - PURPOSE SECTION

Use(s)

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

WARNINGS SECTION

Warnings

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

OTC - DO NOT USE SECTION

Do Not Use

  • on 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 wth eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INSTRUCTIONS FOR USE SECTION

Directions

  • Place enought 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 SAFETY INFORMATION

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients Purified Water, Glyderin, Carbomer, Triethanolamine

DOSAGE & ADMINISTRATION SECTION

Directions

  • 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.

INDICATIONS & USAGE SECTION

Use(s)

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

Directions

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8 oz 73874-0002-1

8 oz8 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12oz 73874-0002-2

12oz12oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

18 oz 73874-0002-3

18oz18oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 gal 73874-0002-4

1gal1gal

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73874-0002-1Hand Sanitizer237 mL in 1 BOTTLE, DISPENSINGLIQUID2371
73874-0002-2Hand Sanitizer355 mL in 1 BOTTLE, DISPENSINGLIQUID3551
73874-0002-3Hand Sanitizer532 mL in 1 BOTTLE, PLASTICLIQUID5321
73874-0002-4Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICLIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73874-0002HAND SANITIZER (ETHYL ALCOHOL) LIQUID [ELEVATION GOURMET, INC.]1Legacy NDC, 4 package rows20200821_acb3d0c1-9e59-63ee-e053-2995a90a699f.zip

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
73874-000273874-0002-1, 73874-0002-2, 73874-0002-3, 73874-0002-4

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

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
acb3d0c1-9e5a-63ee-e053-2995a90a699facb3d0c1-9e59-63ee-e053-2995a90a699f2020-08-12WarningsExact identifier
spl id: acb3d0c1-9e5a-63ee-e053-2995a90a699f
spl set id: acb3d0c1-9e59-63ee-e053-2995a90a699f

Reported adverse events (FAERS/openFDA)#

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