Medi-First® Antiseptic Spray

Manufacturer
Unifirst First Aid Corporation
Effective date
2024-01-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:14:03

Label at a glance#

ProductMedi-First Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose

First aid antiseptic

INDICATIONS & USAGE SECTION

Uses

first aid to help prevent infection in minor cuts, scrapes & burns

WARNINGS SECTION

Warnings

For external use only.

OTC - DO NOT USE SECTION

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

deep or puncture wounds, animal bites, or serious burns

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • the condition persists or gets worse

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

  • clean the affected area
  • spray a small amount of this product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

OTHER SAFETY INFORMATION

Other information

  • store at room temperature
  • you may report a seriuos adverse reaction to this product to 1-800-634-7680

INACTIVE INGREDIENT SECTION

Inactive ingredients

diazolidinyl urea, edetate disodium, glycerin, hypromellose, methylparaben, octoxynol 9, propylene glycol, propylparaben, trolamine, water

OTC - QUESTIONS SECTION

Questions or comments? 1-800-634-7680

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi-First®
Antiseptic Spray
Pump Spray
Benzalkonium Chloride 0.13%
First Aid Antiseptic
​Treats minor cuts, scrapes and abrasions

Helps prevent infection

Store at room temperature

2 FL OZ (59.1 ML)

MF AntisepticMF Antiseptic

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47682-24347682-243-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
0f13e78f-957e-aa53-e063-6294a90a2f37bc908ec0-333a-fcab-e053-2995a90a5da42024-01-16WarningsExact identifier
spl id: 0f13e78f-957e-aa53-e063-6294a90a2f37
spl set id: bc908ec0-333a-fcab-e053-2995a90a5da4

Reported adverse events (FAERS/openFDA)#

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