Midway Lifebuoy Hand Sanitizer Spray

Manufacturer
Midway Importing, Inc.
Effective date
2020-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:23:57

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteriaa on the skin

Dosage and administration

Wet hands thoroughly with product and rub lightly until dry. Do not wipe off or rinse.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteriaa on the skin

Warnings

WARNINGS SECTION

For external use only.Flammable. keep away from heat or flame

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash develops

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 rub lightly until dry. Do not wipe off or rinse.

Other information

OTHER SAFETY INFORMATION

  • May discolor frabrics or surfaces.
  • Store below 105°F (40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Denatonium Benzoate, Glycerin, Purified Water USP

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76095-018-162025-02-24C16284748780-1d6a99b39-5bc8-a426-e053-dadaa90af4c2Midway Lifebuoy Hand Sanitizer Spray
76095-018-162022-01-28C16284748780-1d6a99b39-5bc8-a426-e053-dadaa90af4c2Midway Lifebuoy Hand Sanitizer Spray

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76095-01876095-018-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
2eea2fd0-03de-622d-e063-6394a90a748da93ad7fc-614c-ad7e-e053-2995a90af5752025-02-24WarningsExact identifier
spl set id: a93ad7fc-614c-ad7e-e053-2995a90af575

Reported adverse events (FAERS/openFDA)#

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