Soothing Nerve Therapy

Product NDC: 42346-550
11-digit product format: 423460550
Labeler code: 42346
Product ID: 42346-550_41a30e52-be92-76f6-e063-6294a90a0295
Type: HUMAN OTC DRUG
Nonproprietary name: menthol
Dosage form: LOTION
Route: TOPICAL
Labeler: Wise Consumer Products
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-09-16
Substance: MENTHOL
Active strength: 1.3 g/100g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	42346-550	42346-550-85	D	Discontinued by firm		2026-10-16

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: Soothing Nerve Therapy
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	1.3 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2045268	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
40829d6b-5005-7ec9-e063-6294a90a970e	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
42346-550-85	Soothing Nerve Therapy	85 g in 1 TUBE	LOTION	85		2
42346-550-86	Soothing Nerve Therapy	85 g in 1 TUBE	LOTION	85		2
42346-550-86	Soothing Nerve Therapy	1 in 1 CARTON	LOTION	1		2
42346-550-87	Soothing Nerve Therapy	85 g in 1 TUBE	LOTION	85		2
42346-550-87	Soothing Nerve Therapy	2 in 1 CARTON	LOTION	2		2
42346-550-86	Frankincense and Myrrh Nerve Combo Pack	85 g in 1 TUBE	LOTION	85 g	1.3 g in 100g	1
42346-550-86	Frankincense and Myrrh Nerve Combo Pack	1 in 1 CARTON	LOTION		1.3 g in 100g	1

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 61 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nighttime 4X Medicated Cream	BENZOCAINE	Rite Aid	21645ed1-2dc0-223a-e063-6394a90ab021	2025-11-21	Warnings	Exact identifier application number: M017
4x Medicated Gum Cream	BENZOCAINE	Albertsons	b81a308c-9c30-0e3d-e053-2a95a90a15d2	2025-11-21	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	b0edd9d9-951f-d3dd-e053-2995a90a8d5a	2025-11-21	Warnings	Exact identifier application number: M017
Up up	LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES	Target Corporation	44121d40-86e1-0df6-e063-6294a90aedaf	2025-11-20	Warnings	Exact identifier application number: M017
Up up	PAIN RELIEF ADVANCED HYDROGEL PATCHES	Target Corporation	44128b70-3172-ee37-e063-6294a90a705f	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	f03090fa-f7e6-f53a-e053-2a95a90aa819	2025-11-20	Warnings	Exact identifier application number: M017
HEATING PAIN RELIEF	METHYL SALICYLATE, MENTHOL	SUNSET NOVELTIES, INC	ff073e47-3107-e17e-e053-6294a90a58fa	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	fc8a8f20-97ab-481e-e053-6394a90a3525	2025-11-20	Warnings	Exact identifier application number: M017
MENTHOL	MENTHOL	SUNSET PAIN RELIEF ROLL-ON 3OZ	934d4638-b47b-187d-e053-2995a90ae69d	2025-11-20	Warnings	Exact identifier application number: M017
FOOT PAIN RELIEF ROLL-ON	LIDOCAINE, MENTHOL	Guangzhou Zhupuyou E-commerce Co., Ltd	43edcea0-ab04-f368-e063-6294a90a817a	2025-11-19	Warnings	Exact identifier application number: M017
Absolut Skin Corticosoothe Anti-Itch	HYDROCORTISONE	Absolut Skin Incorporated	deb52218-9176-4aaa-a22f-b66dada6690f	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch Good Neighbor Pharmacy	LIDOCAINE	InterMed Laboratories Private Limited	43f3d189-f6b7-02ed-e063-6394a90afd73	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch HealthA2Z	LIDOCAINE	InterMed Laboratories Private Limited	43f3e288-e828-8130-e063-6394a90a6d44	2025-11-19	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch Leader	LIDOCAINE	InterMed Laboratories Private Limited	42f06914-c8b8-ea9c-e063-6294a90a79e6	2025-11-19	Warnings	Exact identifier application number: M017
CVS Anti-Itch	CAMPHOR, MENTHOL	CVS	87715662-c788-9a8d-e053-2a95a90acb53	2025-11-19	Warnings	Exact identifier application number: M017
Walgreen Anti Itch	CAMPHOR, MENTHOL	Walgreens	b4f47a8d-d4a6-9233-e053-2a95a90afd90	2025-11-19	Warnings	Exact identifier application number: M017
Leader Anti-Itch	CAMPHOR, MENTHOL	LEADER/Cardinal Helath 110, Inc.	9ca985c6-5017-0558-e053-2995a90a8202	2025-11-19	Warnings	Exact identifier application number: M017
CVS Anti-Itch	PRAMOXINE HCL	CVS	87fc476a-5b12-7383-e053-2995a90a530b	2025-11-19	Warnings	Exact identifier application number: M017
Walgreen Anti-Itch	PRAMOXINE HCL	Walgreens	b5f9d1c5-891e-4377-e053-2995a90aa281	2025-11-19	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET PAIN RELIEF	89f5f688-856f-f2df-e053-2995a90a73cf	2025-11-19	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2045268	menthol 1.3 % Topical Lotion	PSN	40829d6b-5005-7ec9-e063-6294a90a970e	2
2045268	menthol 13 MG/ML Topical Lotion	SCD	40829d6b-5005-7ec9-e063-6294a90a970e	2
2045268	menthol 1.3 % Topical Lotion	SY	40829d6b-5005-7ec9-e063-6294a90a970e	2
2045268	menthol 1.3 % Topical Lotion	PSN	471d815c-1c34-e0f8-e063-6294a90aca78	1
2675594	menthol 2 % Topical Oil	PSN	471d815c-1c34-e0f8-e063-6294a90aca78	1
2045268	menthol 13 MG/ML Topical Lotion	SCD	471d815c-1c34-e0f8-e063-6294a90aca78	1
2675594	menthol 20 MG/ML Topical Oil	SCD	471d815c-1c34-e0f8-e063-6294a90aca78	1
2045268	menthol 1.3 % Topical Lotion	SY	471d815c-1c34-e0f8-e063-6294a90aca78	1
2675594	menthol 2 % Topical Oil	SY	471d815c-1c34-e0f8-e063-6294a90aca78	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
42346-550-85	42346055085	85 g in 1 TUBE	85 g				Historical
42346-550-86	42346055086	1 TUBE in 1 CARTON (42346-550-86) / 85 g in 1 TUBE	1 tube	2025-12-17	No	No	Current
42346-550-87	42346055087	2 TUBE in 1 CARTON (42346-550-87) / 85 g in 1 TUBE	2 tube	2025-11-14	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Frankincense and Myrrh Nerve Combo Pack	Wise Consumer Products \| Innovation Labs, Inc.	2025-12-29	HUMAN OTC DRUG LABEL	1
Soothing Nerve Therapy Lotion	Wise Consumer Products \| Innovation Labs, Inc.	2025-10-20	HUMAN OTC DRUG LABEL	2