ELECTRUM NUMB SPRAY ANESTHETIC

Manufacturer
RENU LABORATORIES, INC.
Effective date
2024-03-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:10:10

Label at a glance#

ProductELECTRUM NUMB ANESTHETIC
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure14 sections

Storage and handling

Other Information: Store at 20-25° C (68 - 77°F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Lidocaine HCl 4%

OTC - PURPOSE SECTION

Purpose

Topical Anesthetic

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of pain associated with minor skin procedures

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do Not Use

  • on large areas of the body or on cut, irritated or swollen skin
  • on puncture wounds
  • for more than one week without consulting a doctor

OTC - WHEN USING SECTION

When using this product

  • Use only as directed. Read and follow all directions and warnings on this label.
  • rare cases of serious burns have been reported with products of this type
  • do not bandage or apply local heat (such as heating pads) to the area of use or use with a medicated patch
  • avoid contact with eyes and mucous membranes
  • a transient burning sensation may occur upon applicator but generally disappears in several days

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets

  • If swallowed, get medical help or contact a poison control center right away

DOSAGE & ADMINISTRATION SECTION

Directions

adults and children over 12 years:

  • apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
  • after applying, wash hands with soap and water
  • children 12 years or younger - ask a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aloe Barbadensis Leaf Powder, Benzyl Alcohol, Deionized Water, Disodium EDTA, Ethyl Alcohol SD 40B, Glycerin

STORAGE AND HANDLING SECTION

Other Information:

Store at 20-25° C (68 - 77°F)

OTC - QUESTIONS SECTION

Questions?

574-975-3632

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ELECTRUM SPRAY LABELELECTRUM SPRAY LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1045432lidocaine HCl 4 % Topical SprayPSN3
1045432lidocaine hydrochloride 40 MG/ML Topical SpraySCD3
1045432lidocaine HCl 4 % Topical SpraySY3
1045432lidocaine HCl 4 % Topical Spray GelSY3

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76348-600-04ELECTRUM NUMB ANESTHETIC112 g in 1 BOTTLE, SPRAYSPRAY1123

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76348-600ELECTRUM NUMB ANESTHETIC (LIDOCAINE HCL) SPRAY [RENU LABORATORIES, INC.]3Legacy NDC, 1 package rows20240322_b4ca450f-0833-c299-e053-2995a90afd56.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-60076348-600-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
141d8968-3790-dd6a-e063-6294a90a7ad7b4ca450f-0833-c299-e053-2995a90afd562024-03-20WarningsExact identifier
spl id: 141d8968-3790-dd6a-e063-6294a90a7ad7
spl set id: b4ca450f-0833-c299-e053-2995a90afd56

Reported adverse events (FAERS/openFDA)#

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