Uber Numb

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Uber Numb
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: UBERScientific, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 768f3f0e-1add-404f-b869-00a9f35ad34a
SPL ID: 09d8a838-3a74-c010-e063-6294a90aa31a
Version: 10
Effective date: 2023-11-10
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:24:15

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Uber Numb	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		UBERScientific, LLC	openfda.manufacturer_name
ndc	package	71131-051-02	openfda.package_ndc
ndc	product	71131-051	openfda.product_ndc
ndc11	package	71131005102	derived:openfda.package_ndc
rxcui		1491882	openfda.rxcui
spl id		09d8a838-3a74-c010-e063-6294a90aa31a	id
spl set id		768f3f0e-1add-404f-b869-00a9f35ad34a	set_id
unii		V13007Z41A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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

Reported adverse events (FAERS/openFDA)#

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