Hand Sanitizer

Manufacturer
Comercializadora Lopaza, S.A. de C.V. | Mario Hidalgo
Effective date
2020-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:26

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure16 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 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

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

glycerin, carbomer 940, Trolamine, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 75 mL GelLabel 75 mL Gel75 mL NDC: 78722-123-01

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50000 mL NDC: 78722-123-05 Label 50000 mL GelLabel 50000 mL Gel

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 1000 mL GelLabel 1000 mL Gel1000 mL NDC: 78722-123-02

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 5000 mL GelLabel 5000 mL Gel5000 mL NDC: 78722-123-03

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 200000 mL GelLabel 200000 mL Gel200000 mL NDC: 78722-123-04

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78722-123-01Hand Sanitizer75 mL in 1 BOTTLE, PUMPGEL751
78722-123-02Hand Sanitizer1000 mL in 1 BOTTLE, PUMPGEL10001
78722-123-03Hand Sanitizer1000 mL in 1 BOTTLE, PUMPGEL10001
78722-123-04Hand Sanitizer200000 mL in 1 BOTTLE, PUMPGEL2000001
78722-123-05Hand Sanitizer50000 mL in 1 BOTTLE, PUMPGEL500001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78722-123HAND SANITIZER (ALCOHOL) GEL [COMERCIALIZADORA LOPAZA, S.A. DE C.V.]1Legacy NDC, 5 package rows20200620_a8780f1c-f2c8-bb5e-e053-2995a90a3d50.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
78722-12378722-123-01, 78722-123-02, 78722-123-03, 78722-123-04, 78722-123-05

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
a8780b7e-1eda-cea8-e053-2a95a90a45e1a8780f1c-f2c8-bb5e-e053-2995a90a3d502020-06-19WarningsExact identifier
spl id: a8780b7e-1eda-cea8-e053-2a95a90a45e1
spl set id: a8780f1c-f2c8-bb5e-e053-2995a90a3d50

Reported adverse events (FAERS/openFDA)#

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