FDA.reportPublic FDA data

Medi-First Alcohol Wipes

Manufacturer
Unifirst First Aid Corporation
Effective date
2023-03-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:35:24

Label at a glance#

ProductMedi-First Alcohol Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Isopropyl Alcohol, 70%

OTC - PURPOSE SECTION

Purpose

Anticeptic

INDICATIONS & USAGE SECTION

Uses

  • for preparation of the skin prior to injection
  • first aid to help prevent infection in minor cuts, scrapes and burns

WARNINGS SECTION

Warnings

  • for external use only
  • flammable, keep away from fire or flame

OTC - DO NOT USE SECTION

Do not use

  • with electrocautery procedures
  • in the eyes. If contact occurs, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation and redness develops
  • 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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • wipe injection site vigorously and discard
  • apply to cut, scrape or burn and discard after single use

OTHER SAFETY INFORMATION

Other information

  • store at room temperature 59º-86ºF (15º-30ºC)
  • tamper evident sealed packets
  • do not use any open or torn packets

INACTIVE INGREDIENT SECTION

Inactive ingredients

purified water

OTC - QUESTIONS SECTION

Questions or comments?
1-800-634-7680

Medi-First Alcohol Wipes Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi-First®

Alcohol Wipes

Sterile

Isopropyl Alcohol 70%

First aid to help prevent infection in minor cuts, scrapes and burns.

Product #33133

100 per box

MF AlcoholMF Alcohol

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-33147682-331-33, 47682-331-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
f5d6ee54-1fa1-c87b-e053-2a95a90a14eca83647fa-fadd-a3fa-e053-2995a90a64502023-03-01WarningsExact identifier
spl id: f5d6ee54-1fa1-c87b-e053-2a95a90a14ec
spl set id: a83647fa-fadd-a3fa-e053-2995a90a6450

Reported adverse events (FAERS/openFDA)#

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