Numbing 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: Numbing Cream
Generic name: LIDOCAINE
Manufacturer: 100 KARMA INC
Product type: HUMAN OTC DRUG
SPL set ID: 35884644-d017-eda3-e063-6394a90a1f6c
SPL ID: 35884644-d018-eda3-e063-6394a90a1f6c
Version: 1
Effective date: 2025-05-19
Source export date: 2026-10-30
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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:31:27

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		Numbing Cream	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		100 KARMA INC	openfda.manufacturer_name
ndc	package	85569-001-01	openfda.package_ndc
ndc	product	85569-001	openfda.product_ndc
ndc11	package	85569000101	derived:openfda.package_ndc
rxcui		1421893	openfda.rxcui
spl id		35884644-d018-eda3-e063-6394a90a1f6c	id
spl set id		35884644-d017-eda3-e063-6394a90a1f6c	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 Do not use this product if Pregnant or breastfeeding, ask a health professional before use. If there is any allergic reaction to this product. In case of accidental overdose, get medical help, or contact the poison control center immediately. Only take the recommended daily dosage unless otherwise instructed by a doctor. Some individuals may experience allergic reactions to the ingredients contained in this product. Stop using and ask a doctor If discomfort persists for 7 days. The symptoms being treated do not subside or if redness irritation swelling, pain, or other symptoms develop or increase. Keep out of reach of children Avoid contact with eyes. In case of accidental ingestion, seek medical attention immediately.

Reported adverse events (FAERS/openFDA)#

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