FDA.reportPublic FDA data

Electrum Numb Foam

Manufacturer
RENU LABORATORIES, LLC
Effective date
2025-04-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:59:48

Label at a glance#

ProductElectrum Numb Foam
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections

Indications and uses

can be used instead of soap and water to help clean minor cuts, scrapes, and burns. For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, tattoo, dermarolling, electrolysis, microblading and piercing. Temporarily relieves pain and itch while helping prevent infection Directions Shake Well before each use. Apply 2 to 3 pumps of foam soap and gently rub into skin. ...

Label contents#

Full prescribing information#

Uses

INDICATIONS & USAGE SECTION

can be used instead of soap and water to help clean minor cuts, scrapes, and burns.

  • For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, tattoo, dermarolling, electrolysis, microblading and piercing.
  • Temporarily relieves pain and itch while helping prevent infection

Directions

  • Shake Well before each use. Apply 2 to 3 pumps of foam soap and gently rub into skin. Leave it on for 5 to 10 minutes. Rinse off gently with running water or wipe with a clean paper towel. Use before, during and after the procedure. Keep bottle tightened to keep product fresh and effective. Adults and children 2 years old and older. Use to clean minor cuts, scrapes and burns by thoroughly washing with water. Rinse and air dry. Use no more than 3 times a day.
  • Children under two years of age, ask a doctor

RECENT MAJOR CHANGES SECTION

Directions for Use were added.

WARNINGS SECTION

For external use only

  • avoid contact with eyes
  • do not exceed recommended dosage unless directed by a doctor

OTC - DO NOT USE SECTION

Do not use

  • in the eyes or apply to large areas of body
  • longer than 1 week unless directed by a doctor
  • in large quantities particularly over raw surfaces or blistered areas
  • ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

OTC - STOP USE SECTION

Stop Use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Allantoin, Aloe Barbadensis (Aloe) Powder, Arnica Montana (Arnica) Extract, Caprylyl Glycol, Cocoamidopropyl Betaine, Deionized Water, Disdoium Cocoamphodiacetate, Glycerin, Hexylene Glycol, Phenoxyethanol, Sodium Chloride.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children:

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - QUESTIONS SECTION

Questions? 574-975-3632

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Lidocaine HCL 4%

OTC - PURPOSE SECTION

Purpose

Topical anesthetic

First aid antiseptic

STATEMENT OF IDENTITY SECTION

ELECTRUM NUMB FOAM FOAMING ANESTHETIC

DOSAGE & ADMINISTRATION SECTION

Directions

Shake well before each use. Apply 2 to 3 pumps of foam soap and gently rub into skin. Leave it on for 5 to 10 minutes.

Rinse off gently with running water or wipe with a clean paper towel. Use before, during and after the procedure.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

foam labelfoam label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2604567lidocaine hydrochloride 4 % Medicated Liquid SoapPSN6
2604567lidocaine hydrochloride 40 MG/ML Medicated Liquid SoapSCD6
2604567lidocaine hydrochloride 4 % Medicated Liquid SoapSY6

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76348-596-172024-03-21C16284748780-11030e365-33d6-111a-e063-dadaa90a10e2Electrum Numb Foam
76348-596-172024-01-30C16284748780-11030e365-33d6-111a-e063-dadaa90a10e2Electrum Numb Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76348-596-17Electrum Numb Foam48 mL in 1 BOTTLE, PUMPSOAP486

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76348-596ELECTRUM NUMB FOAM (LIDOCAINE HCI) SOAP [RENU LABORATORIES, LLC]6Current NDC, Legacy NDC, 1 package rows20250427_c8472932-28b7-9189-e053-2a95a90a44df.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-59676348-596-17

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
SODIUM CHLORIDE451W47IQ8XIACT
ALLANTOIN344S277G0ZIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ARNICA MONTANAO80TY208ZWIACT
CAPRYLYL GLYCOL00YIU5438UIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
GLYCERINPDC6A3C0OXIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Electrum Numb FoamLIDOCAINE HCIRENU LABORATORIES, LLCc8472932-28b7-9189-e053-2a95a90a44df2025-04-25WarningsExact identifier
ndc (package): 76348-596-17
ndc (product): 76348-596
ndc11 (package): 76348059617
spl id: 33a12d5b-1eac-7b76-e063-6294a90a04eb
spl set id: c8472932-28b7-9189-e053-2a95a90a44df

Reported adverse events (FAERS/openFDA)#

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