Electrum Numb Foam

Product NDC: 76348-596
Requested package NDC: 76348-596-17
11-digit product format: 763480596
Labeler code: 76348
Product ID: 76348-596_33a12d5b-1eac-7b76-e063-6294a90a04eb
Type: HUMAN OTC DRUG
Nonproprietary name: Lidocaine HCI
Dosage form: SOAP
Route: TOPICAL
Labeler: RENU LABORATORIES, LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-07-29
Substance: LIDOCAINE HYDROCHLORIDE
Active strength: 1.92 g/48mL
Pharmacologic classes: Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2024-03-11 06:39 UTC · source 2024-03-08	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2022-04-09 23:13 UTC · source 2022-04-08	E	Excluded after deficient or non-compliant submission was not corrected	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	E	Excluded after deficient or non-compliant submission was not corrected	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	E	Excluded after deficient or non-compliant submission was not corrected	`8dfbde2a14a4…`	`c9ff85d89658…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Electrum Numb Foam
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LIDOCAINE HYDROCHLORIDE	1.92 g/48mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
V13007Z41A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2604567	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c8472932-28b7-9189-e053-2a95a90a44df	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76348-596-17	2024-03-21	C162847	48780-1	1030e365-33d6-111a-e063-dadaa90a10e2	Electrum Numb Foam
76348-596-17	2024-01-30	C162847	48780-1	1030e365-33d6-111a-e063-dadaa90a10e2	Electrum Numb Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76348-596-17	Electrum Numb Foam	48 mL in 1 BOTTLE, PUMP	SOAP	48		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76348-596	ELECTRUM NUMB FOAM (LIDOCAINE HCI) SOAP [RENU LABORATORIES, LLC]	6	Current NDC, Legacy NDC, 1 package rows	20250427_c8472932-28b7-9189-e053-2a95a90a44df.zip

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 117 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MYCO Clinic Pain Relief	MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	604a30c9-2306-47a1-bd31-94b63639dd90	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	0b489420-3b5c-43c5-aab4-0e3720acf9ce	2024-11-20	Warnings	Exact identifier application number: M017
MYCO Clinic Pain Relief	CAMPHOR, MENTHOL	Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	dd906129-a787-4352-856d-d7a915031a6e	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Arthritis Pain Relief Cream	HISTAMINE DIHYDROCHLORIDE	Walgreens Company	80d3031a-7fa9-4f5b-b85e-c7c6ef314801	2024-11-20	Warnings	Exact identifier application number: M017
Anti-Itch Medicated Maximum Strength	BENZOCAINE AND RESORCINOL	Walgreens Company	7fd86dcb-edef-4d0d-b389-7ecea595fe67	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Pain Relief	BENZOCAINE	Walgreens Company	7cee7234-32cd-4bf3-8a6c-0882585eec7f	2024-11-20	Warnings	Exact identifier application number: M017
Walgreens Advanced Scar Gel	ADVANCED SCAR GEL	Walgreens Company	2c040475-a124-485c-933e-66b452f5ab46	2024-11-20	Warnings	Exact identifier application number: M017
LidoPro Pain Relief	CAPSAICIN AND LIDOCAINE	Clinic Pharma	274611ea-7fc2-ba3f-e063-6294a90aa50f	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief Pad	BENZOCAINE	Acme United Corporation	5087cbbd-1bbe-62ed-e054-00144ff8d46c	2024-11-19	Warnings	Exact identifier application number: M017
Sting Relief Pad	BENZOCAINE, ISOPROPYL ALCOHOL	Acme United Corporation	6bb9a782-2394-4c8c-e053-2991aa0a08d4	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Sting Relief	BENZOCAINE	Acme United Corporation	697127d1-c02e-16d2-e053-2a91aa0a39fd	2024-11-19	Warnings	Exact identifier application number: M017
First Aid Only Hydrocortisone 1% Anti-Itch	HYDROCORTISONE	Acme United Corporation	e5597b11-b08e-99e1-e053-2a95a90a15a5	2024-11-19	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Roll-on Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	4115f0ac-e12a-4e59-94f5-a47dcc7f8766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Cold Therapy Pain Relieving Analgesic	MENTHOL, UNSPECIFIED FORM	Wal-Mart Stores, Inc.	ac6c2112-8692-4628-97d8-3a5a9f509766	2024-11-18	Warnings	Exact identifier application number: M017
Equate Odor-Free Therapy Arthritis Analgesic	TROLAMINE SALICYLATE	Wal-Mart Stores, Inc.	1d73e7b6-c7f9-4680-b3e3-a954b91e1863	2024-11-18	Warnings	Exact identifier application number: M017
First Aid Only Burn	LIDOCAINE HYDROCHLORIDE	Acme United Corporation	9af39fcd-0a57-26d0-e053-2a95a90a99a0	2024-11-17	Warnings	Exact identifier application number: M017
First Aid Only First Aid/Burn	LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE	Acme United Corporation	caa67a05-bdbd-c380-e053-2995a90a0bf1	2024-11-17	Warnings	Exact identifier application number: M017
Meijer Pain Lidocaine Plus Relieving Analgesic	BENZYL ALCOHOL AND LIDOCAINE HYDROCHLORIDE	Meijer Distribution, Inc	b7385140-3f63-4cbc-b557-de1d29d1ea36	2024-11-15	Warnings	Exact identifier application number: M017
Signature Care Hydrocortisone	HYDROCORTISONE	Safeway	c6b9c4e1-bab8-490d-8c00-c43377ad0857	2024-11-15	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Walgreen Company	1a9b8b4c-3e15-49e6-af91-76ed0dc0829e	2024-11-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V13007Z41A	LIDOCAINE HYDROCHLORIDE	6108-05-0	LIDOCAINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2604567	lidocaine hydrochloride 4 % Medicated Liquid Soap	PSN	c8472932-28b7-9189-e053-2a95a90a44df	6
2604567	lidocaine hydrochloride 40 MG/ML Medicated Liquid Soap	SCD	c8472932-28b7-9189-e053-2a95a90a44df	6
2604567	lidocaine hydrochloride 4 % Medicated Liquid Soap	SY	c8472932-28b7-9189-e053-2a95a90a44df	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76348-596-17	76348059617	48 mL in 1 BOTTLE, PUMP (76348-596-17)	48 ml	2021-07-29	0000-00-00	No	No	Current