FDA.reportPublic FDA data

Hand Clean antibacterial gel

Manufacturer
Materias Primas Medina Campos SA de CV.
Effective date
2020-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:08

Label at a glance#

ProductHand Clean antibacterial gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

to decrease bacteria that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to  dry without wiping for children under 6, use only under adult supervision not recommended for infants   

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire

Warning

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to 
  • dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants   

Other Information

SPL UNCLASSIFIED SECTION

  • do not store above 105° F
  • may discolor some fabrics
  • harmful to wood finishes and platics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

colorless, transparent gel, water 10-50%, glicerina (moisturizer) 0.1-1%, triethanol-amine 1-5%, pH:6.5-7.5 stability: 6 months biodegradable, phosphate free.

Package Labeling:1L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:500L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:250L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79674-00179674-001-02, 79674-001-03, 79674-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERETH-8EL2NFK7352IACT
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
ce2987b6-7787-32c8-e053-2a95a90a95eeae2edcd6-8090-a68e-e053-2995a90a14542021-10-12WarningsExact identifier
spl set id: ae2edcd6-8090-a68e-e053-2995a90a1454

Reported adverse events (FAERS/openFDA)#

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