Deeveeant Numb

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: Deeveeant Numb
Generic name: LIDOCAINE
Manufacturer: Valekista Limited
Product type: HUMAN OTC DRUG
SPL set ID: 2d7b39cc-4f1b-4414-b129-88c56e159aba
SPL ID: 577a6fed-7e6a-47c6-af44-bcfbc4675126
Version: 1
Effective date: 2017-07-06
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:23:27

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		part348	openfda.application_number
brand name		Deeveeant Numb	openfda.brand_name
generic name		LIDOCAINE	openfda.generic_name
manufacturer name		Valekista Limited	openfda.manufacturer_name
ndc	package	71383-014-02	openfda.package_ndc
ndc	product	71383-014	openfda.product_ndc
ndc11	package	71383001402	derived:openfda.package_ndc
rxcui		1421893	openfda.rxcui
spl id		577a6fed-7e6a-47c6-af44-bcfbc4675126	id
spl set id		2d7b39cc-4f1b-4414-b129-88c56e159aba	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 Avoid contact with eyes Not for prolonged use Do not use in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clears up and occurs again within a few days rash or irritation develops, persists or increases If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away: 800-222-1222

Reported adverse events (FAERS/openFDA)#

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