FDA.reportPublic FDA data

Nox-A-Sting

Manufacturer
Honeywell Safety Products USA, Inc | Safetec of America, Inc.
Effective date
2024-01-19
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
legacy-cache
Hydrated at
2026-08-01 21:13:50

Label at a glance#

ProductSTING RELIEF PAD
Active ingredientLIDOCAINE HYDROCHLORIDE, ALCOHOL
Label structure9 sections

Indications and uses

prevent infection in minor scrapes, and temporary relief of itching of insect bites

Dosage and administration

adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily. children under 2 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

in each wipe:

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Topical pain relief

Uses

INDICATIONS & USAGE SECTION

  • prevent infection in minor scrapes, and temporary relief of itching of insect bites

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from open fire or flame

Do not use

OTC - DO NOT USE SECTION

  • over large areas of the body
  • in eyes
  • over raw or blistered areas

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if conditions worsen or persist for more than 7 days or clear up and occur again within a few days

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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
  • children under 2 years of age: consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, menthol, and purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Sting Relief label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sting ReliefSting Relief

Nox-A-Sting label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nox-A-StingNox-A-Sting

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-07330498-0733-00, 0498-0733-34, 0498-0733-10
0498-17330498-1733-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
MENTHOLL7T10EIP3AIACT
WATER059QF0KO0RIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
MENTHOLL7T10EIP3AIACT
WATER059QF0KO0RIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
ALCOHOL3K9958V90MACTIB

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
1a169508-a8af-0103-e063-6394a90ae79061040741-c870-1ad5-e053-2991aa0a3ab42024-06-04WarningsExact identifier
spl set id: 61040741-c870-1ad5-e053-2991aa0a3ab4

Reported adverse events (FAERS/openFDA)#

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