Numpot 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: Numpot Topical Anesthetic
Generic name: LIDOCAINE, PETROLATUM
Manufacturer: Unit Dose, Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 9143b50b-7d76-4545-aa2e-1bb77ffb44ae
SPL ID: 0814bc6d-5504-8353-e063-6394a90a0e16
Version: 4
Effective date: 2023-10-19
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:43

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		Numpot Topical Anesthetic	openfda.brand_name
generic name		LIDOCAINE, PETROLATUM	openfda.generic_name
manufacturer name		Unit Dose, Ltd.	openfda.manufacturer_name
ndc	package	67194-018-01	openfda.package_ndc
ndc	product	67194-018	openfda.product_ndc
ndc11	package	67194001801	derived:openfda.package_ndc
rxcui		1733863	openfda.rxcui
spl id		0814bc6d-5504-8353-e063-6394a90a0e16	id
spl set id		9143b50b-7d76-4545-aa2e-1bb77ffb44ae	set_id
unii		4T6H12BN9U	openfda.unii
unii		98PI200987	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

WARNING: External use only. Keep out of eyes. Allergic reactions can occur. STOP USE & ASK A DOCTOR: If condition worsens or does not improve within 7 days If redness, irritation, pain, swelling or other symptoms develop or increase If bleeding occurs. KEEP OUT OF REACH OF CHILDREN: If swallowed get medical help or contact a Poison Control Center ASAP.

Reported adverse events (FAERS/openFDA)#

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