Hand Sanitizing Gel Frota

Manufacturer
Integradora de Espectáculos de Guadalajara, S.A. de C.V.
Effective date
2021-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:57:33

Label at a glance#

ProductHand Sanitizing Gel Frota
Active ingredientALCOHOL
Label structure6 sections

Indications and uses

* Hand sanitizer to help redice bacterial on the skin that could of cause* recomendended for repeated use.

Dosage and administration

Place enough product in your palm to throughly over your hands * Rub hands together briskly until dry*children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

purspose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

* Hand sanitizer to help redice bacterial on the skin that could of cause* recomendended for repeated use.

Warnings

WARNINGS SECTION

Flammable, keep away from fire of flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes throughly with wáter.

Stop uses and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasis.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

I swallowed, get medical help or contact a posion control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to throughly over your hands * Rub hands together briskly until dry*children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, carbomer, triethanolamine y fragance..

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
81356-00081356-000-01

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
ec0847af-088a-3dfc-e053-2995a90a6bb7b8670880-5585-8722-e053-2a95a90aad482022-10-27WarningsExact identifier
spl set id: b8670880-5585-8722-e053-2a95a90aad48

Reported adverse events (FAERS/openFDA)#

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