Tempo Sting Relief Pad

Manufacturer
Tempo Medical Products
Effective date
2020-01-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:02:51

Label at a glance#

ProductTempo BZK Towelette
Active ingredientBENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, BENZOCAINE
Label structure3 sections

Label contents#

Full prescribing information#

Product Label for NDC 71756-8050-1 (BZK Towelette)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71756-8050-1 POUCH71756-8050-1 POUCH

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open pouch, unfold and use. Discard after single use.

Warnings

WARNINGS SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water, camphor

Do Not Use / Stop Use / Use

INDICATIONS & USAGE SECTION

(Do not use)

  • On irritated skin or over large areas of the body
  • If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

Cleansing of hands, face and body. Air dries in seconds.

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 immediately.

Purpose

OTC - PURPOSE SECTION

Antiseptic Cleanser

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% v/v

Product Label for NDC 71756-8010-1 (Alcohol Prep Pad)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71756-8010-1 POUCH71756-8010-1 POUCH

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe injection site and discard after single use.

Warnings

WARNINGS SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

Do Not Use / Stop Use / Use

INDICATIONS & USAGE SECTION

(Do not use)

  • With electrocautery procedures
  • If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

For preparation of the skin prior to an injection

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 immediately.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Product Label for NDC 71756-8090-1 (Sting Relief Pad)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

71756-8090-1 POUCH71756-8090-1 POUCH

Directions

DOSAGE & ADMINISTRATION SECTION

Clean intended area with pad and discard after single use.

Warnings

WARNINGS SECTION

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

Do Not Use / Stop Use / Use

INDICATIONS & USAGE SECTION

(Do not use)

  • With electrocautery procedures
  • If contact occurs with eyes, flush eyes with water

(Stop use)

if irritation and redness develop. Consult your physician if the condition persists.

(Use)

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

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 immediately.

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic (Benzocaine)

Antiseptic (Isopropyl Alcohol)

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6% v/v

Isopropyl Alcohol 70% v/v

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN6
809206benzocaine 6 % / isopropyl alcohol 70 % Medicated PadPSN6
797544isopropyl alcohol 70 % Medicated PadPSN6
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD6
809206benzocaine 60 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated PadSCD6
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD6
1038558benzalkonium chloride 0.13 % Topical ClothSY6
1038558benzalkonium chloride 0.13 % Topical SwabSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY6
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY6
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY6
809206benzocaine 6 % / isopropyl alcohol 70 % Medicated PadSY6
809206benzocaine 6 % / isopropyl alcohol 70 % Topical SwabSY6
797544isopropyl alcohol 70 % Medicated PadSY6
797544isopropyl alcohol 70 % Topical ClothSY6
797544isopropyl alcohol 70 % Topical SwabSY6

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71756-8010-1Tempo Alcohol Prep Pad0.45 mL in 1 POUCHSWAB0.456
71756-8050-1Tempo BZK Towelette1.5 mg in 1 POUCHCLOTH1.56
71756-8090-1Tempo Sting Relief Pad0.45 mg in 1 POUCHSWAB0.456

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71756-8010TEMPO BZK TOWELETTE (BENZALKONIUM CHLORIDE) CLOTH TEMPO ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB TEMPO STING RELIEF PAD (BENZOCAINE, ISOPROPYL ALCOHOL) SWAB [TEMPO MEDICAL PRODUCTS]6Legacy NDC, 1 package rows20200109_59a609e7-4da3-525b-e053-2991aa0a90e2.zip
71756-8050TEMPO BZK TOWELETTE (BENZALKONIUM CHLORIDE) CLOTH TEMPO ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB TEMPO STING RELIEF PAD (BENZOCAINE, ISOPROPYL ALCOHOL) SWAB [TEMPO MEDICAL PRODUCTS]6Legacy NDC, 1 package rows20200109_59a609e7-4da3-525b-e053-2991aa0a90e2.zip
71756-8090TEMPO BZK TOWELETTE (BENZALKONIUM CHLORIDE) CLOTH TEMPO ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB TEMPO STING RELIEF PAD (BENZOCAINE, ISOPROPYL ALCOHOL) SWAB [TEMPO MEDICAL PRODUCTS]6Legacy NDC, 1 package rows20200109_59a609e7-4da3-525b-e053-2991aa0a90e2.zip

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
71756-805071756-8050-1
71756-801071756-8010-1
71756-809071756-8090-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
9bab182c-1b68-cebb-e053-2a95a90abc2a59a609e7-4da3-525b-e053-2991aa0a90e22020-01-08WarningsExact identifier
spl id: 9bab182c-1b68-cebb-e053-2a95a90abc2a
spl set id: 59a609e7-4da3-525b-e053-2991aa0a90e2

Reported adverse events (FAERS/openFDA)#

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