TheraCare Lidocaine Pain Relief

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: TheraCare Lidocaine Pain Relief
Generic name: LIDOCAINE
Manufacturer: Veridian Healthcare
Product type: HUMAN OTC DRUG
SPL set ID: ee8cd550-64ee-432e-98e5-b68083179a3c
SPL ID: 47a9429f-b59b-667f-e063-6394a90a5f68
Version: 1
Effective date: 2026-01-05
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:50

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		TheraCare Lidocaine Pain Relief	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Veridian Healthcare	openfda.manufacturer_name
ndc	package	71101-941-06	openfda.package_ndc
ndc	product	71101-941	openfda.product_ndc
ndc11	package	71101094106	derived:openfda.package_ndc
spl id		47a9429f-b59b-667f-e063-6394a90a5f68	id
spl set id		ee8cd550-64ee-432e-98e5-b68083179a3c	set_id
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

Warnings For external use only. Flammable. Keep away from fire or flame. Do not use while smoking. Do not punture or incinerate. Contents under pressure When using this product When using this product Avoid contact with eyes. do not use in large quatities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if condition worsens or if symptoms persist for more than 7 days or clear up and reoccur within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away If pregnant or breastfeeding Ask a helth professional before use

Reported adverse events (FAERS/openFDA)#

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