FDA.reportPublic FDA data

Medi-First Sting Relief

Manufacturer
Unifirst First Aid Corporation
Effective date
2025-09-08
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:12:56

Label at a glance#

ProductMedi-First Sting Relief
Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Dosage and administration

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily. Children under 2 years: CXonsult physician.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6% w/v

Isopropyl alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • in the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation, redness or other symptoms develop
  • the 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

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily.

Children under 2 years: CXonsult physician.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-634-7680

Medi-First Sting Relief Wipes Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi-First®

Sting Relief Wipes

Benzocaine/ Isopropyl Acohol

Topical Anesthetic/ Antiseptic

Product # 23112

NET CONTENTS: 10 wipes per box

Mf StingRelief Wipes LabelMf StingRelief Wipes Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadPSN7
895749benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated PadSCD7
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadSY7
895749benzocaine 6 % / isopropyl alcohol 60 % Topical SwabSY7

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-234-12Medi-First Sting Relief0.6 mL in 1 PACKETSWAB0.67
47682-234-12Medi-First Sting Relief10 in 1 BOXSWAB107
47682-234-99Medi-First Sting Relief0.6 mL in 1 PACKETSWAB0.67

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
47682-23447682-234-99, 47682-234-12

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
BENZOCAINEU3RSY48JW5ACTIB
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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 Sting ReliefBENZOCAINE 6%, ISOPROPYL ALCOHOL 60%Unifirst First Aid Corporation6e610821-b030-930b-e053-2a91aa0a66f92025-09-08WarningsExact identifier
ndc (package): 47682-234-12
ndc (package): 47682-234-99
ndc (product): 47682-234
ndc11 (package): 47682023499
ndc11 (package): 47682023412
spl id: 3e4cef3b-1393-fc54-e063-6294a90ad5f2
spl set id: 6e610821-b030-930b-e053-2a91aa0a66f9

Reported adverse events (FAERS/openFDA)#

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