FDA.reportPublic FDA data

Reduvir Hand sanitizer

Manufacturer
Culta S.A. de C.V.
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:36

Label at a glance#

ProductReduvir Hand sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. For children under 6, use only under adult supervision. Not recommended for infants.

Storage and handling

Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Purpose: Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease. Recommend for repeated use. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable. Keep away from heat and flame

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes flush thoroughly with water.
Avoid contact with broken skin. Do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritations and redness develop
  • condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • For children under 6, use only under adult supervision. Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 105F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 mL NDC: 80358-001-05

500 mL500 mL

1000 mL NDC: 80358-001-10

1000 mL1000 mL

3785 mL NDC: 80358-001-37

3785 mL3785 mLBack LabelBack Label

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
80358-00180358-001-10, 80358-001-05, 80358-001-37

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
POLYACRYLIC ACID (800000 MW)D0I6NSZ87UIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT

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
ae6e5767-5636-9c52-e053-2995a90a29dca8fef253-f2f8-0d91-e053-2a95a90ac5ca2020-09-03WarningsExact identifier
spl set id: a8fef253-f2f8-0d91-e053-2a95a90ac5ca

Reported adverse events (FAERS/openFDA)#

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