Hand Sanitizer Gel

Manufacturer
Vara Home Usa Llc | Yangzhou Jiefeiao Tourism-plastic Products Chemical Plant
Effective date
2020-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:55

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106F (41F). May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

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

Flammable. Keep away from heat or flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes.

Stop use and ask medical doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

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 in your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 106F (41F).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Triethanolamine, Carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 79060-002-01

PDPPDP

60 mL NDC:79060-002-02

PDPPDP

1000 mL NDC: 79060-002-03

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79060-002-012022-01-28C16284748780-1d6a99b39-dc72-a426-e053-dadaa90af4c2Hand Sanitizer Gel
79060-002-022022-01-28C16284748780-1d6a99b39-dc72-a426-e053-dadaa90af4c2Hand Sanitizer Gel
79060-002-032022-01-28C16284748780-1d6a99b39-dc72-a426-e053-dadaa90af4c2Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79060-002-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
79060-002-02Hand Sanitizer60 mL in 1 BOTTLEGEL601
79060-002-03Hand Sanitizer1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79060-002HAND SANITIZER (ALCOHOL) GEL [VARA HOME USA LLC]1Legacy NDC, 3 package rows20200617_a7ea48eb-4f70-6fd6-e053-2995a90a0f9e.zip

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
79060-00279060-002-01, 79060-002-02, 79060-002-03
74742-004

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
a7ea6312-06c5-b73f-e053-2995a90a37d6a7ea48eb-4f70-6fd6-e053-2995a90a0f9e2020-06-12WarningsExact identifier
spl id: a7ea6312-06c5-b73f-e053-2995a90a37d6
spl set id: a7ea48eb-4f70-6fd6-e053-2995a90a0f9e

Reported adverse events (FAERS/openFDA)#

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