FDA.reportPublic FDA data

DUAL ANESTHETIC NUMBING

Manufacturer
LEIBOVICH EDWARD PERSOANA FIZICA AUTORIZATA
Effective date
2026-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:48:48

Label at a glance#

ProductDUAL ANESTHETIC NUMBING
Active ingredientLIDOCAINE, BENZOCAINE, TROLAMINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients | Purpose
Lidocaine 4% ........................ Anesthetic
Benzocaine 20% ...................... Anesthetic
Trolamine 0.067% .................... Anesthetic

OTC - PURPOSE SECTION

Uses
For temporary pain relief for minor cuts, burns, skin scrapes

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

For temporary pain relief for minor cuts, burns, skin scrapes

Store at temperatures 59°F (15°–30°C)

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aloe Vera, Chamomile Extract, Vitamin E, Glycerin, Menthol, Lecithin

WARNINGS SECTION

Warnings
For external use only

When using this product
Do not contact with eyes.

Keep out of reach of children
If redness, irritation, swelling, or pain persists beyond 7 day, or recurs or if swallowed

If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

For temporary pain relief for minor cuts, burns, skin scrapes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dual Aesthetic Numbing Cream

Full PackingFull PackingBox 2Box 2Box PicBox PicDrugs FactsDrugs Facts

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87320-0001-1DUAL ANESTHETIC NUMBING50 g in 1 BOXCREAM501

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87320-000187320-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHAMOMILEFGL3685T2XIACT
ALOE VERA LEAF OILJQ7YW886UQIACT
VITAMIN E POLYETHYLENE GLYCOL SUCCINATEO03S90U1F2IACT
LIDOCAINE98PI200987ACTIB
BENZOCAINEU3RSY48JW5ACTIB
TROLAMINE9O3K93S3TKACTIB

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
DUAL ANESTHETIC NUMBINGDUAL ANESTHETIC NUMBINGLEIBOVICH EDWARD PERSOANA FIZICA AUTORIZATA4c1de25d-2586-f0cd-e063-6294a90aff362026-03-03WarningsExact identifier
ndc (package): 87320-0001-1
ndc (product): 87320-0001
ndc11 (package): 87320000101
spl id: 4c1de25d-2587-f0cd-e063-6294a90aff36
spl set id: 4c1de25d-2586-f0cd-e063-6294a90aff36

Reported adverse events (FAERS/openFDA)#

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