Treatonic 5% Lidocaine Cream

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: Treatonic 5% Lidocaine Cream
Generic name: 5% LIDOCAINE CREAM
Manufacturer: 100 KARMA INC
Product type: HUMAN OTC DRUG
SPL set ID: 49e6b69f-bd6e-b415-e063-6394a90a8e65
SPL ID: 58dba5f4-60c1-55e2-e063-6394a90ac2d7
Version: 2
Effective date: 2026-08-12
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:54:13

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		M015	openfda.application_number
brand name		Treatonic 5% Lidocaine Cream	openfda.brand_name
generic name		5% LIDOCAINE CREAM	openfda.generic_name
manufacturer name		100 KARMA INC	openfda.manufacturer_name
ndc	package	85569-014-01	openfda.package_ndc
ndc	product	85569-014	openfda.product_ndc
ndc11	package	85569001401	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		58dba5f4-60c1-55e2-e063-6394a90ac2d7	id
spl set id		49e6b69f-bd6e-b415-e063-6394a90a8e65	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

For external use 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 no t put this product into the rectum by using fingers or any mechanical device or applicatior. An allergic reaction occurs Symptom does not improve or if redness, irritation, swelling, pain or other symptom develop or increase. Ask a health professional before use. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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