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: Sainite Trading Shenzhen Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 49fcbe81-34b6-5906-e063-6294a90aa65b
SPL ID: 49fcbe81-34b7-5906-e063-6294a90aa65b
Version: 1
Effective date: 2026-02-04
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:54

Harmonized routes table
Harmonized routes
CUTANEOUS

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		Numbing Cream	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Sainite Trading Shenzhen Co., Ltd.	openfda.manufacturer_name
ndc	package	82929-011-01	openfda.package_ndc
ndc	product	82929-011	openfda.product_ndc
ndc11	package	82929001101	derived:openfda.package_ndc
rxcui		1534792	openfda.rxcui
spl id		49fcbe81-34b7-5906-e063-6294a90aa65b	id
spl set id		49fcbe81-34b6-5906-e063-6294a90aa65b	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. 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. Do not put this product into the rectum by using fingers or any mechanical device or applicator. Certain persons can develop allergic reactions to ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor. Keep out of reach of children if swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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