Inkeeze Original Numb Professional Numbing Gel

Manufacturer
Indelicare, LLC
Effective date
2021-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:52

Label at a glance#

ProductInkeeze Original B Numb
Active ingredientLIDOCAINE
Label structure7 sections

Indications and uses

External Use Only: For the temporary relief of local itching and discomfort in the perianal area.

Dosage and administration

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting with an appropriate cleansing pad. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

PURPOSE:

OTC - PURPOSE SECTION

Topical Anesthetic

USES:

INDICATIONS & USAGE SECTION

External Use Only: For the temporary relief of local itching and discomfort in the perianal area.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Alcohol, Benzyl Alcohol Carbomer, Citric Acid, Ethoxydiglycol, Propylene Glycol, Purified Water.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or by patting with an appropriate cleansing pad. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.

WARNINGS SECTION

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended daily dosage unless directed by a doctor. In case of bleeding, consult a doctor promptly. Do not put this product into the rectum by using fingers or any mechanical device or applicator. Certain persons can develop allergic reactions to ingredients in this product. If the symptoms being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor.

WHEN USING THIS PRODUCT:

OTC - WHEN USING SECTION

you may notice temporary blanching or redness of the skin where gel is applied.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1010057lidocaine HCl 5 % Topical GelPSN1
1010057lidocaine hydrochloride 0.05 MG/MG Topical GelSCD1
1010057lidocaine hydrochloride 5 % Topical GelSY1

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82022-000-002023-01-30C16284748780-1f386c649-b3a9-0266-e053-dadaa90a7c1aInkeeze Original Numb Professional Numbing Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82022-000-00Inkeeze Original B Numb29.5 mL in 1 TUBEGEL29.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82022-000INKEEZE ORIGINAL B NUMB (LIDOCAINE) GEL [INDELICARE, LLC]1Legacy NDC, 1 package rows20210813_c95e1f0c-06c9-a021-e053-2995a90aa704.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82022-00082022-000-00

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
c95e09e8-24e3-2a0b-e053-2a95a90a24f5c95e1f0c-06c9-a021-e053-2995a90aa7042021-08-12WarningsExact identifier
spl id: c95e09e8-24e3-2a0b-e053-2a95a90a24f5
spl set id: c95e1f0c-06c9-a021-e053-2995a90aa704

Reported adverse events (FAERS/openFDA)#

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