ETADERM 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: ETADERM Numbing Cream
Generic name: LIDOCAINE
Manufacturer: NUEPHASE LLC
Product type: HUMAN OTC DRUG
SPL set ID: 5292c6ff-b878-4e71-878b-4bf08207612e
SPL ID: 46b82621-0092-2ac8-e063-6394a90a5e82
Version: 4
Effective date: 2025-12-24
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:27:34

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		ETADERM Numbing Cream	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		NUEPHASE LLC	openfda.manufacturer_name
ndc	package	84180-001-04	openfda.package_ndc
ndc	package	84180-001-01	openfda.package_ndc
ndc	product	84180-001	openfda.product_ndc
ndc11	package	84180000104	derived:openfda.package_ndc
ndc11	package	84180000101	derived:openfda.package_ndc
rxcui		1366789	openfda.rxcui
spl id		46b82621-0092-2ac8-e063-6394a90a5e82	id
spl set id		5292c6ff-b878-4e71-878b-4bf08207612e	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 When using this product ▪ do not get into eyes. ▪ 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. Stop use and ask a doctor if ▪ condition worsens or does not improve within 7 days. ▪ in case of bleeding, consult a doctor promptly ▪ 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. If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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