MEDI-FIRST First Aid Antiseptic

Manufacturer
Ultra Distributors Inc
Effective date
2025-04-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:58:47

Label at a glance#

ProductMEDI-FIRST First Aid Antiseptic
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

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

Dosage and administration

clean affected area & spray 1 to 3 times daily may be covered with a sterile bandage not to be used on children under 12 years of age

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • near eyes or mucous membranes
  • on deep or puncture wounds, animal bites, or serious burns
  • over large areas of the body
  • more than one week unless directed by a doctor

Stop use and ask a doctor

OTC - STOP USE SECTION

if condition persists or gets worse

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

  • clean affected area & spray 1 to 3 times daily
  • may be covered with a sterile bandage
  • not to be used on children under 12 years of age

Inactive ingredients

INACTIVE INGREDIENT SECTION

ethyl alcohol, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-634-7680

SPL UNCLASSIFIED SECTION

Treats minor cuts, scrapes and abrasions

Helps prevent infection

Store at 68°-77°F (20°-25°C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN2
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD2
1039012benzalkonium chloride 0.13 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78495-122-012025-04-07C16284748780-12cef2736-a700-d83d-e063-dadaa90ab31f78495-122
78495-122-012025-01-30C16284748780-12cef2736-a700-d83d-e063-dadaa90ab31f78495-122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78495-122-01MEDI-FIRST First Aid Antiseptic59.1 mL in 1 BOTTLE, PUMPSPRAY59.12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78495-122MEDI-FIRST FIRST AID ANTISEPTIC (BENZALKONIUM CHLORIDE) SPRAY [ULTRA DISTRIBUTORS INC]2Current NDC, Legacy NDC, 1 package rows20250409_b6efaca5-49d0-b000-e053-2995a90ab9aa.zip

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
78495-12278495-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALCOHOL3K9958V90MIACT

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
MEDI-FIRST First Aid AntisepticBENZALKONIUM CHLORIDEUltra Distributors Incb6efaca5-49d0-b000-e053-2995a90ab9aa2025-04-07WarningsExact identifier
ndc (package): 78495-122-01
ndc (product): 78495-122
ndc11 (package): 78495012201
spl id: 3239abbd-8033-7f52-e063-6294a90a8740
spl set id: b6efaca5-49d0-b000-e053-2995a90ab9aa

Reported adverse events (FAERS/openFDA)#

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