FDA.reportPublic FDA data

Bite and Sting relief

Manufacturer
Top care | Product Quest Mfg.
Effective date
2018-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:13

Label at a glance#

ProductBite and Sting relief
Active ingredientBenzocaine
Label structure7 sections

Indications and uses

For temporarily relief of pain and itching associated with insect bites

Label contents#

Full prescribing information#

Active ingredients                   Purpose

OTC - ACTIVE INGREDIENT SECTION

Benzocaine                                5.00%

Uses

INDICATIONS & USAGE SECTION

For temporarily relief of pain and itching associated with insect bites

WarningFor external use only

WARNINGS SECTION

When using this product avoid contact with eyes and mucous membranes

Stop use and ask a doctor if 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
If product is swallowed, get medical help or contact a Poison Control Center right away
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 the affected area nor mre than 3 to 4 times daily. Children under 2 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water
PEG-2 Stearate
PEG-2 Stearate SE
SD Alcohol 40
Polyethylene
Hydrocortisone
Methylparaben
Aloe Barbadensis Leaf Extract
Propylparaben
Chamomilla Recutita (Matricaria) Flower Extract
Propylene Glycol
Diazolidinyl Urea
Disodium EDTA
Olea Europaea (Olive) Fruit Oil
Camphor
Menthol
Mentha Piperita (Peppermint) Oil
Eugenia Caryophyllus (Clove) Flower Oil
Papain

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198494benzocaine 5 % Topical CreamPSN1
198494benzocaine 50 MG/ML Topical CreamSCD1
198494benzocaine 5 % Topical CreamSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
15bd4439-874a-4934-9954-248e5455d460Product name120260310
9962b773-9f2e-22cc-0032-535e48ac417bProduct name320250724
56bb0587-1bf2-48b2-9d93-fc9f59d1eeb2Product name120250325
4d56e8eb-d741-d4a5-de3f-2bab1af75a60Product name720220608
626d7260-31b5-4412-84fd-579746adb6b3Product name120210513
8a011600-5e61-4c59-ab7b-54ab658a3b71Product name220181127
a919621a-248d-3c7a-1084-9f9ce286fdfdProduct name220181009
e7d5a174-836b-a0af-b014-cb0826c69ddcProduct name220181004
fcce390d-6460-4701-87cf-940d8800a1c3Product name220180212
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
bf065fa6-1e3b-e4c3-0bde-2dc842ceeea1Product name220150218
02657a3f-1489-66ea-f740-5ab9524e57d7Product name120140508
26f3d783-2cc1-4327-e77d-71804cf675a2Product name120140508
36fdc54c-bbeb-981e-8a53-4d768e283892Product name120140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
61e59a42-186b-9f4b-aec3-fb49a6debc31Product name120140508
705740e1-dee5-2610-c5a3-4c59cd9d62afProduct name120140508
7bdc4804-3832-c0df-e519-72b6d47c9792Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
abaf203f-619e-f265-559f-8c81af5cb1c2Product name120140508
acc4d8bb-0e29-e9f8-65f8-31e94184a9c0Product name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
bfd28ffb-d550-3fe9-f65b-10bcb7f971fdProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508
fe21f3fd-a378-0654-1972-db3c3b64470eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
36800-718-022020-01-31C16284748780-19d75b9d0-ba3d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-718-02Bite and Sting relief50 g in 1 TUBECREAM501
36800-718-02Bite and Sting relief1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-718BITE AND STING RELIEF (BENZOCAINE - 5.00%) CREAM [TOP CARE]1Legacy NDC, 2 package rows20180710_bb232a27-9732-46b6-a452-9c7d226d1bb1.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
36800-71836800-718-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
BenzocaineU3RSY48JW5ACTIB
Water059QF0KO0RIACT
PEG-2 Stearate94YQ11Y95FIACT
ALCOHOL3K9958V90MIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
HydrocortisoneWI4X0X7BPJIACT
MethylparabenA2I8C7HI9TIACT
ALOE VERA LEAFZY81Z83H0XIACT
PropylparabenZ8IX2SC1OHIACT
CHAMOMILEFGL3685T2XIACT
Propylene Glycol6DC9Q167V3IACT
Diazolidinyl UreaH5RIZ3MPW4IACT
EDETATE DISODIUM7FLD91C86KIACT
OLIVE OIL6UYK2W1W1EIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
MentholL7T10EIP3AIACT
PeppermintV95R5KMY2BIACT
CLOVE OIL578389D6D0IACT
PapainA236A06Y32IACT

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
d48bb363-9f43-4a3c-8833-fd618e3a9507bb232a27-9732-46b6-a452-9c7d226d1bb12018-07-09WarningsExact identifier
spl id: d48bb363-9f43-4a3c-8833-fd618e3a9507
spl set id: bb232a27-9732-46b6-a452-9c7d226d1bb1

Reported adverse events (FAERS/openFDA)#

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