Hand Sanitizer

Manufacturer
GIA EVOLUTION SA DE CV
Effective date
2020-07-02
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 23:19:56

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 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 70% 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

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

purified water USP, glycerin, carbomer, triethanolamine.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

29.5 mL NDC: 77231-010-01 2929

59 mL NDC: 77231-010-02 5959

237 mL NDC: 77231-010-03 237237

500 mL NDC: 77231-010-04 500mL500mL

946 mL NDC: 77231-010-05 3232

3785 mL NDC: 77231-010-06 galongalon

200000 mL NDC: 77231-010-08 200L200L

1000000 mL NDC: 77231-010-07 1000L1000L

20000000 mL NDC: 77231-010-09 2000020000

2000 mL NDC: 77231-010-10

PDP 2LPDP 2L

8000 mL NDC: 77231-010-11

PDP 4-8LPDP 4-8L

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN7
581662ethanol 0.7 ML/ML Topical GelSCD7
581662ethanol 70 % Topical GelSY7
581662ethyl alcohol 70 % Topical GelSY7

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77231-010-01Hand Sanitizer29.57 mL in 1 BOTTLE, UNIT-DOSEGEL29.577
77231-010-02Hand Sanitizer59.15 mL in 1 BOTTLEGEL59.157
77231-010-03Hand Sanitizer236.59 mL in 1 BOTTLEGEL236.597
77231-010-04Hand Sanitizer500 mL in 1 BOTTLEGEL5007
77231-010-05Hand Sanitizer946.35 mL in 1 BOTTLEGEL946.357
77231-010-06Hand Sanitizer3785.41 mL in 1 CONTAINERGEL3785.417
77231-010-07Hand Sanitizer1000000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKGEL10000007
77231-010-08Hand Sanitizer200000 mL in 1 DRUMGEL2000007
77231-010-09Hand Sanitizer20000000 mL in 1 TANKGEL200000007
77231-010-10Hand Sanitizer2000 mL in 1 BOTTLEGEL20007
77231-010-11Hand Sanitizer8000 mL in 1 BOXGEL80007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77231-010HAND SANITIZER (ALCOHOL) GEL [GIA EVOLUTION SA DE CV]7Legacy NDC, 11 package rows20200703_a57ce7c0-d561-cd4c-e053-2995a90a46bc.zip

Products#

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

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

NDC Codes#

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
a979cdc4-13e3-3b2b-e053-2995a90a3992a57ce7c0-d561-cd4c-e053-2995a90a46bc2020-07-02WarningsExact identifier
spl id: a979cdc4-13e3-3b2b-e053-2995a90a3992
spl set id: a57ce7c0-d561-cd4c-e053-2995a90a46bc

Reported adverse events (FAERS/openFDA)#

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