FDA.reportPublic FDA data

ALL CLEAR

Manufacturer
CALIDAD Y SERVICIO VIAN, S.A. DE C.V. | CALIDAD Y SERVICIO VIAN S.A DE C.V.
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:20:35

Label at a glance#

ProductALL CLEAR
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

DIRECTIONS Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry. Children under six years of age should be supervised when using this product.

Storage and handling

Other Information Store at 1°C - 30°C (34 °F - 86 °F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

Warnings

  • For External use only Flammable
  • Keep away from fire or flame

Stop Use

OTC - STOP USE SECTION

Stop use and ask doctor

  • If irritation and redness persist for more then 72 hours.

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

In case of accidental ingestion, seek medicalattention or contact a poison control center immediately

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to decrease bacteria on the skin
  • Recommended for repeated use

Directions

INSTRUCTIONS FOR USE SECTION

DIRECTIONS

  • Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under six years of age should be supervised when using this product.

Storage

STORAGE AND HANDLING SECTION

Other Information

  • Store at 1°C - 30°C (34 °F - 86 °F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

  • Carbomer, Glycerin, Triethanolamine, Water

ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under six years of age should be supervised when using this product.

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DPDDPD

500ML

NDC: 79787-001-01

NDC : 77070-700-80

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79787-00179787-001-01

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
ACRYLIC ACIDJ94PBK7X8SIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
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
af774de2-4ed7-283f-e053-2a95a90ae587ab0dfcf2-d64b-76e7-e053-2995a90a6b342020-09-16WarningsExact identifier
spl set id: ab0dfcf2-d64b-76e7-e053-2995a90a6b34

Reported adverse events (FAERS/openFDA)#

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