FDA.reportPublic FDA data

Uber Numb Cream

Manufacturer
UBERScientific, LLC
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 00:02:14

Label at a glance#

ProductUber Numb
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure7 sections

Indications and uses

For the Temporary relief of pain and discomfort associated with anorectal disorders

Dosage and administration

 For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly, Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product. Adults and children 12 years and older: Apply externally up to 6 times per day. Consult a Doctor Children under 12: 

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCL (5%)

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the Temporary relief of pain and discomfort associated with anorectal disorders

Warnings:

WARNINGS SECTION

For external ues only. 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. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact the Poison Control Center immediately

Directions:

DOSAGE & ADMINISTRATION SECTION

 For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly, Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product. Adults and children 12 years and older:

Apply externally up to 6 times per day.

Consult a Doctor Children under 12: 

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Allantoin Gel, Deionized Water, Benzyl Alcohol, Carbomer, Propylene Glycol, Sodium Polyacrylate, Tocopheryl Acetate (Vitamin E), Triethanolamine

Distributed by:

SPL UNCLASSIFIED SECTION

UberScientific LLC 838 E High St. Ste 271

Lexington, KY 40502

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1491882lidocaine HCl 5 % Topical CreamPSN10
1491882lidocaine hydrochloride 50 MG/ML Topical CreamSCD10
1491882lidocaine hydrochloride 5 % Topical CreamSY10

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
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
71131-051-02Uber Numb57 g in 1 JARCREAM5710
71131-051-02Uber Numb1 in 1 CARTONCREAM110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71131-051UBER NUMB (LIDOCAINE HYDROCHLORIDE) CREAM [UBERSCIENTIFIC, LLC]10Current NDC, Legacy NDC, 2 package rows20231116_768f3f0e-1add-404f-b869-00a9f35ad34a.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
71131-05171131-051-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZYL ALCOHOLLKG8494WBHIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TROLAMINE9O3K93S3TKIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR

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
Uber NumbLIDOCAINE HYDROCHLORIDEUBERScientific, LLC768f3f0e-1add-404f-b869-00a9f35ad34a2023-11-10WarningsExact identifier
ndc (package): 71131-051-02
ndc (product): 71131-051
ndc11 (package): 71131005102
spl id: 09d8a838-3a74-c010-e063-6294a90aa31a
spl set id: 768f3f0e-1add-404f-b869-00a9f35ad34a

Reported adverse events (FAERS/openFDA)#

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