FDA.reportPublic FDA data

Lanco Antiseptic Hand Sanitizer

Manufacturer
Lanco Manufacturing, Corp.
Effective date
2020-12-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:11

Label at a glance#

ProductLanco Antiseptic Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

to decrease bacteria on the skin that could cause diseases 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 on the skin that could cause diseases
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands
Flammable, keep away from heat, fire or flame.

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 
  • Condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or 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 plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glyceryl caprylate/caprate, glycerin, carboxyl vinyl polymer, propylene glycol, triethanolamine

Questions?

OTC - QUESTIONS SECTION

+1-787-736-4221

You may also report serious side effects to this phone number

Mon-Fri 9:00 AM - 5:00 PM

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80522-001-012023-01-30C16284748780-1f386c649-e47c-0266-e053-dadaa90a7c1aLanco Antiseptic Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80522-001-01Lanco Antiseptic Hand Sanitizer3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80522-001LANCO ANTISEPTIC HAND SANITIZER (ALCOHOL) LIQUID [LANCO MANUFACTURING, CORP.]1Legacy NDC, 1 package rows20201231_b60b967b-f120-336b-e053-2a95a90acef5.zip

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
80522-00180522-001-01

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
WATER059QF0KO0RIACT
GLYCERYL MONOCAPRYLOCAPRATEG7515SW10NIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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
b60b967b-f121-336b-e053-2a95a90acef5b60b967b-f120-336b-e053-2a95a90acef52020-12-09WarningsExact identifier
spl id: b60b967b-f121-336b-e053-2a95a90acef5
spl set id: b60b967b-f120-336b-e053-2a95a90acef5

Reported adverse events (FAERS/openFDA)#

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