FDA.reportPublic FDA data

Bite and Sting Medicated Relief Pads

Manufacturer
CVS | Product Quest Mfg
Effective date
2018-02-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:41

Label at a glance#

ProductBite and Sting Medicated Relief Pads CVS
Active ingredientBENZOCAINE
Label structure9 sections

Indications and uses

For temporarily relief of pain and itching associated with minor cuts, scrapes and minor burns

Label contents#

Full prescribing information#

Active ingredient                   Purpose

OTC - ACTIVE INGREDIENT SECTION

Benzocaine - 5.00%                Pain Relief

Uses

INDICATIONS & USAGE SECTION

For temporarily relief of pain and itching associated with minor cuts, scrapes and minor burns

WarningsFor external use only

WARNINGS SECTION

Flammable: ​ do not use while smoking or near heat or flame

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes
  • use only as directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens
• symptoms last 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 the children
In case of accidental ingestion, seek professional or contact a Poison Control Center immediately.

Direction

DOSAGE & ADMINISTRATION SECTION

• adults and children 2 years of age and older: Apply to affected area, not more than 3 to 4 times daily
• children under 2 years of age: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Ascorbic Acid, Camphor, Chamomilla Recutita (Matricaria) Flower Extract, Cholecalciferol, Diisopropyl Adipate,
Eugenia Caryophyllus (Clove) Flower Oil, Fragrance, Mentha Piperita (Peppermint) Oil, Octyldodecanol, Olea Europaea (Olive) Fruit Oil,
PEG-8 Dimethicone, Propylene Glycol, Pyridoxine HCl, Retinyl Palmitate, SD Alcohol 40, Silica, Sodium Propoxyhydroxypropyl Thiosulfate Silica,
Tocopheryl Acetate, Zea Mays (Corn) Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1927647benzocaine 5 % Medicated PadPSN1
1927647benzocaine 50 MG/ML Medicated PadSCD1
1927647benzocaine 5 % Medicated PadSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
5e18e798-5614-cf5c-0185-38b1cb77a093Product name220160822
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69842-856-032020-01-31C16284748780-19d75b9d0-3d4e-f424-e053-dadaa90a57ceDrag Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-856-03Bite and Sting Medicated Relief PadsCVS72 g in 1 JARLIQUID721

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-856BITE AND STING MEDICATED RELIEF PADS CVS (BENZOCAINE - 5.00%) LIQUID [CVS]1Legacy NDC, 1 package rows20180223_ad0ab5f3-b4e9-4097-b2bd-a1ead230b514.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69842-85669842-856-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOCAINEU3RSY48JW5ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
CHAMOMILEFGL3685T2XIACT
Cholecalciferol1C6V77QF41IACT
Diisopropyl AdipateP7E6YFV72XIACT
CLOVE OIL578389D6D0IACT
PEPPERMINT OILAV092KU4JHIACT
Octyldodecanol461N1O614YIACT
OLIVE OIL6UYK2W1W1EIACT
PEG-8 DimethiconeGIA7T764ODIACT
Propylene Glycol6DC9Q167V3IACT
PYRIDOXINE HYDROCHLORIDE68Y4CF58BVIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
Alcohol3K9958V90MIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
Sodium Propoxyhydroxypropyl Thiosulfate Silica208G222332IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CORN OIL8470G57WFMIACT

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
2d47401b-c1cd-46c6-be26-1e3340e9c926ad0ab5f3-b4e9-4097-b2bd-a1ead230b5142018-02-23WarningsExact identifier
spl id: 2d47401b-c1cd-46c6-be26-1e3340e9c926
spl set id: ad0ab5f3-b4e9-4097-b2bd-a1ead230b514

Reported adverse events (FAERS/openFDA)#

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