RECOVERY Numbing

Product NDC: 76348-980
11-digit product format: 763480980
Labeler code: 76348
Product ID: 76348-980_36eb74ef-8d4f-be0a-e063-6394a90a6552
Type: HUMAN OTC DRUG
Nonproprietary name: Lidocaine HCl
Dosage form: SPRAY
Route: TOPICAL
Labeler: Renu Laboratories, LLC
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-08-01
Substance: LIDOCAINE HYDROCHLORIDE
Active strength: 5.9 g/118mL
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 · 26 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	76348-980-04	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	76348-980-04	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	76348-980-04	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	76348-980-04	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	76348-980-04	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	76348-980-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	76348-980-04	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	76348-980-04	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	76348-980-04	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	76348-980-04	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	76348-980-04	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	76348-980-04	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	76348-980-04	`1332a3947898…`	`d4bfe170f9cd…`

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: RECOVERY Numbing
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LIDOCAINE HYDROCHLORIDE	5.9 g/118mL

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
1545290	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
e4e05cae-56a6-b2b3-e053-2a95a90a104b	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
76348-980-04	2025-06-06	C162847	48780-1	1030e365-484a-111a-e063-dadaa90a10e2	RECOVERY NUMBING SPRAY
76348-980-04	2024-01-30	C162847	48780-1	1030e365-484a-111a-e063-dadaa90a10e2	RECOVERY NUMBING SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76348-980-04	RECOVERY Numbing	118 mL in 1 BOTTLE, SPRAY	SPRAY	118		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76348-980	RECOVERY NUMBING (LIDOCAINE HCL) SPRAY [RENU LABORATORIES, INC.]	1	Current NDC, Legacy NDC, 1 package rows	20220819_e4e05cae-56a6-b2b3-e053-2a95a90a104b.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 13 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GoodSense Hemorrhoidal Pain Relief	GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL	Perrigo Direct, Inc	2e5f699d-45e8-6451-e063-6394a90a8ad8	2025-07-20	Warnings	Exact identifier application number: M015
Good Sense Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	L. Perrigo Company	379f8738-a871-4b09-abd1-c86386dfee04	2025-07-15	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Pads	WITCH HAZEL	Walmart, Inc.	6dd8d3d9-5109-4869-917b-9521e9ba1ed0	2025-07-14	Warnings	Exact identifier application number: M015
Nikzon Hemorrhoidal	GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE	Genomma Lab USA	8f9a9939-2c99-489f-b597-9a51ec2684f9	2025-07-14	Warnings	Exact identifier application number: M015
ReVIVOL-XR	PHENYLEPHRINE HYDROCHLORIDE	Unipack LLC	2950fe83-a2a4-4ed4-b645-69d6fd2381ae	2025-07-13	Warnings	Exact identifier application number: M015
medicated wipes	WITCH HAZEL	Meijer Distribution Inc.	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	2025-07-11	Warnings	Exact identifier application number: M015
hemorrhoidal pads	WITCH HAZEL	Meijer Distribution Inc.	53e39d22-a89e-4f95-8c64-abeb50f72ce7	2025-07-11	Warnings	Exact identifier application number: M015
INVIGOR OH	LIDOCAINE	Natureplex LLC	7c7b536d-e41a-4017-9df9-982e2e9cfe4e	2025-07-10	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Cream with Aloe	GLYCERIN, PHENYLEPHINE HCI, PRAMOXINE HCI, PETROLATUM	Chain Drug Marketing Association	396ea654-8be1-591a-e063-6294a90a11e2	2025-07-08	Warnings	Exact identifier application number: M015
PREPARATION H SOOTHING RELIEF ANTI-ITCH	HYDROCORTISONE	Haleon US Holdings LLC	d6148d77-ef6f-4552-b5ba-43b429923f19	2025-07-07	Warnings	Exact identifier application number: M015
Rectal Care Cream	RECTAL CARE CREAM	Allegiant Health	ce585082-ad39-4b6f-a756-0d9a81a13eb8	2025-07-07	Warnings	Exact identifier application number: M015
Bisacodyl Laxative	BISACODYL LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cb0386-a662-6893-e063-6294a90aa71a	2025-07-03	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM	Trifecta Pharmaceuticals Usa Llc	38cf4e43-280b-eb96-e063-6294a90a5949	2025-07-02	Warnings	Exact identifier application number: M015
TN Dickinsons Medicated Cooling Foam Hemorrhoidal Relief	WITCH HAZEL	Dickinson Brands Inc.	deca8ae2-53a3-4c90-aa10-45354e2cdab8	2025-06-27	Warnings	Exact identifier application number: M015
Glycerin Laxative	GLYCERIN LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cc266a-196f-16ce-e063-6394a90a24af	2025-06-20	Warnings	Exact identifier application number: M015
Phenylephrine Hemorrhoidal	HEMORRHOIDAL SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35ccb320-e902-3d1a-e063-6294a90a68d5	2025-06-20	Warnings	Exact identifier application number: M015
ProCure Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Twin Med LLC	37a4cc43-0d53-f1bf-e063-6394a90a2dc9	2025-06-15	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	HEMORRHOIDAL PAIN RELIEF OINTMENT	Neilmed Pharmaceuticals Inc.	374d89b6-9305-9adf-e063-6394a90adb32	2025-06-11	Warnings	Exact identifier application number: M015
Dermoplast Post Partum	BENZOCAINE	Advantice Health, LLC	374dced3-6527-b458-e063-6394a90a911e	2025-06-11	Warnings	Exact identifier application number: M015
foster and thrive hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	Strategic Sourcing Services LLC	fb3bc359-b06b-4995-aa68-0117a639dff2	2025-06-11	Warnings	Exact identifier application number: M015

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
1545290	lidocaine HCl 5 % Topical Spray	PSN	e4e05cae-56a6-b2b3-e053-2a95a90a104b	2
1545290	lidocaine hydrochloride 50 MG/ML Topical Spray	SCD	e4e05cae-56a6-b2b3-e053-2a95a90a104b	2
1545290	lidocaine hydrochloride 5 % Topical Spray	SY	e4e05cae-56a6-b2b3-e053-2a95a90a104b	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
76348-980-04	76348098004	118 mL in 1 BOTTLE, SPRAY (76348-980-04)	118 ml	2022-08-01	0000-00-00	No	No	Current