FDA.reportPublic FDA data

HANDS SANITIZER GEL 70% ETHYL ALCOHOL

Manufacturer
Pinturas De Alto Rendimiento, S.A. De C.V.
Effective date
2020-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:19:15

Label at a glance#

ProductHANDS SANITIZER 70 ETHYL ALCOHOL
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Dispense directly on hands and rub thoroughly. For children should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

  • For external use only. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

  • Flammable, keep away from heat, sparks, open flame, hot surfaces - No smoking.
  • Avoid contact with eyes.
  • If contact occurs, rinse thoroughly with water.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Dispense directly on hands and rub thoroughly.
  • For children should be supervised while using this product.

Inactive ingredient(s):

INACTIVE INGREDIENT SECTION

Water (aqua), glycerin, carbomero, triethanolamine.

SPL UNCLASSIFIED SECTION

This product does not replace washing with soap and water.  Product of Mexico

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79673-000-012022-02-16C16284748780-1d6a99b39-5df1-a426-e053-dadaa90af4c2HANDS SANITIZER GEL 70% ETHYL ALCOHOL
79673-000-012022-01-28C16284748780-1d6a99b39-5df1-a426-e053-dadaa90af4c2HANDS SANITIZER GEL 70% ETHYL ALCOHOL

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
79673-00079673-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

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
d824ef25-b93b-7c45-e053-2a95a90a14639f7d4b9d-2439-4f1c-9c0b-55199f8cad7f2022-02-16WarningsExact identifier
spl set id: 9f7d4b9d-2439-4f1c-9c0b-55199f8cad7f

Reported adverse events (FAERS/openFDA)#

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