Uber Numb Topical Anesthetic

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 Topical Anesthetic
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: UberScientific, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4939a547-c94b-3350-e054-00144ff88e88
SPL ID: 09d8b426-919e-1129-e063-6394a90ae9cd
Version: 7
Effective date: 2023-11-10
Source export date: 2026-10-27
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:06:04

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M015	openfda.application_number
brand name		Uber Numb Topical Anesthetic	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		UberScientific, LLC	openfda.manufacturer_name
ndc	package	71131-797-04	openfda.package_ndc
ndc	product	71131-797	openfda.product_ndc
ndc11	package	71131079704	derived:openfda.package_ndc
rxcui		1871453	openfda.rxcui
rxcui		1491882	openfda.rxcui
spl id		09d8b426-919e-1129-e063-6394a90ae9cd	id
spl set id		4939a547-c94b-3350-e054-00144ff88e88	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 use only. Use only as directed. When using this product, do not exceed the recommended daily dosage unless directed by a doctor. Do not insert this product into rectum using fingers or any mechanical device. Keep out of reach of children. Children under 12 should consult physician prior to use. Stop using this product if: Symptoms worsen or does not improve within seven days Bleeding occurs. *Redness, irritation, swelling, pain or other symptoms develop.

Reported adverse events (FAERS/openFDA)#

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