FDA.reportPublic FDA data

Limpiel

Manufacturer
Ecodeli Comercial SA de CV
Effective date
2020-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:56

Label at a glance#

ProductLimpiel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Superviser children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30 °C (59-86 °F) Avoid freezing and excesive heat above 40 °C (104 °F)

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.

Superviser children under 6 years of age when using this product to avoid swallowing.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat of flame.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, propylene glycol, glycerin, polyacrylic acid, triethanolamine.

Use

INDICATIONS & USAGE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Purpose

OTC - PURPOSE SECTION

Antiseptic, hand sanitizer

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75 % v/v

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age

On open skin wounds

OTC - WHEN USING SECTION

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

If irritation or rash occurs. These may be signs of a serious condition.

STORAGE AND HANDLING SECTION

Store between 15-30 °C (59-86 °F)

Avoid freezing and excesive heat above 40 °C (104 °F)

Package label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LimpielLimpiel5000 ml NDC 76880-001-01

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76880-00176880-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
POLYACRYLIC ACID (8000 MW)73861X4K5FIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
b67489c3-c54d-3b41-e053-2995a90a4823a43e63b4-d78b-cbf2-e053-2995a90afc2b2020-12-14WarningsExact identifier
spl set id: a43e63b4-d78b-cbf2-e053-2995a90afc2b

Reported adverse events (FAERS/openFDA)#

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