Sooth-a-Sting

Manufacturer
HART Health
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:32:45

Label at a glance#

ProductSooth-a-Sting
Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

Temporarily relief of pain and itching associated with insect bites insect stings

Dosage and administration

Adults and chldren 2 years of age and older: remover stinger carefully gently wipe on and around point of insect puncture do not reuse wipe dispose of wipe properly Children under 2 years of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6%

Isopropyl Alcohol 60%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Topical Antiseptic

Uses

INDICATIONS & USAGE SECTION

Temporarily relief of pain and itching associated with

  • insect bites
  • insect stings

Warnings

WARNINGS SECTION

For external use only

do not get in eyes

not for prolonged use

FLAMMABLE keep away from heat and flame

Allergy alert: A severe allertic reaction to insect bites and stings may require life support measures. In such cases, immediately call 911 or your local emergency provider.

Do not use

OTC - DO NOT USE SECTION

  • more than 3 to 4 times daily
  • in or near the eyes or over large portions of the body

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms last more than 3 days
  • unusual redness, swelling, rash, or other irriation occurs

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 1-800-222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and chldren 2 years of age and older:

  • remover stinger carefully
  • gently wipe on and around point of insect puncture
  • do not reuse wipe
  • dispose of wipe properly

Children under 2 years of age:

  • ask a doctor

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadPSN6
895749benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated PadSCD6
895749benzocaine 6 % / isopropyl alcohol 60 % Medicated PadSY6
895749benzocaine 6 % / isopropyl alcohol 60 % Topical SwabSY6

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

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
50332-004850332-0048-1, 50332-0048-7

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 · Source PDF

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
Sooth-a-StingBENZOCAINE, ISOPROPYL ALCOHOLHART Healthc0e7d661-a9c9-4656-a516-57552848ebe82026-01-12WarningsExact identifier
ndc (package): 50332-0048-7
ndc (package): 50332-0048-1
ndc (product): 50332-0048
ndc11 (package): 50332004801
ndc11 (package): 50332004807
spl id: 8f3dc183-0405-4191-a584-82e7983966e4
spl set id: c0e7d661-a9c9-4656-a516-57552848ebe8

Reported adverse events (FAERS/openFDA)#

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