Relief Recovery

Product NDC: 33346-3400
11-digit product format: 333463400
Labeler code: 33346
Product ID: 33346-3400_46a85c17-af03-ba2f-e063-6394a90a74aa
Type: HUMAN OTC DRUG
Nonproprietary name: Methyl salicylate
Dosage form: OIL
Route: TOPICAL
Labeler: Mayway Corporation
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-05-18
Substance: METHYL SALICYLATE; MENTHOL; CAMPHOR OIL; CAPSICUM OLEORESIN
Active strength: 20; 8; 4; .25 g/50mL; g/50mL; g/50mL; g/50mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	33346-3400		I	Inactivated by FDA		2026-10-21
excluded package	package	33346-3400	33346-3400-1	I	Inactivated by FDA		2026-10-21

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 · 36 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	33346-3400-1	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	33346-3400-1	`f5e01cc5f278…`	`a2eaf40c39c3…`
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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`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	33346-3400-1	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	33346-3400-1	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	33346-3400-1	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	33346-3400-1	`bd6a592717d7…`	`303034d00443…`

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: Relief Recovery
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
METHYL SALICYLATE	20 g/50mL
MENTHOL	8 g/50mL
CAMPHOR OIL	4 g/50mL
CAPSICUM OLEORESIN	.25 g/50mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
LAV5U5022Y	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup
75IZZ8Y727	Internal UNII lookup
UW86K581WY	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
27afd45e-2dc5-d099-e063-6394a90ad2b7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
473d070d-1c38-488e-b991-c4d1bf45aab8	Product name	1	20210201
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
33346-3400-1	2022-01-28	C162847	48780-1	d6a99b3a-01c3-a426-e053-dadaa90af4c2	Relief+Recovery

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
33346-3400-1	Relief Recovery	1 in 1 BOX	OIL	1	21
33346-3400-2	Relief Recovery	50 mL in 1 VIAL, GLASS	OIL	50	21
33346-3400-3	Relief Recovery	50 mL in 1 BOTTLE	OIL	50	2
33346-3400-4	Relief Recovery	1 in 1 BOX	OIL	1	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
33346-3400	RELIEF RECOVERY (METHYL SALICYLATE) OIL [MAYWAY CORPORATION]	21	Current NDC, Legacy NDC, 2 package rows	20210101_d68a2b74-551a-476e-a6db-7771ebfadfb2.zip
33346-3400	RELIEF RECOVERY (METHYL SALICYLATE) OIL [MAYWAY CORPORATION]	1	Current NDC, Legacy NDC, 2 package rows	20241126_27afd45e-2dc5-d099-e063-6394a90ad2b7.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 81 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MedPride Medicated Body Powder Powder	MENTHOL, ZINC OXIDE	Shield Line LLC	cdb2fa5b-cf04-c876-e053-2a95a90a187c	2025-08-15	Warnings	Exact identifier application number: M017
Burn	LIDOCAINE	HART Health	c5ff392a-e788-43e0-91ea-5e0f8420586c	2025-08-15	Warnings	Exact identifier application number: M017
Stopain Clinical	MENTHOL	Troy Manufacturing, Inc.	40df30ba-41ba-42b7-93fe-4183b57bdb00	2025-08-14	Warnings	Exact identifier application number: M017
Signature Care Aloe Vera Gel with Lidocaine	LIDOCAINE	Safeway, Inc.	d5069622-97b1-ba12-e053-2a95a90a7268	2025-08-14	Warnings	Exact identifier application number: M017
METHYL SALICYLATE 25%	METHYL SALICYLATE	Oncora Pharma, LLC	3c4bc55d-6582-3b5e-e063-6394a90a994c	2025-08-13	Warnings	Exact identifier application number: M017
Lidocaine 3%	LIDOCAINE HCL 3%	PureTek Corporation	3bc94d52-fe52-9fd6-e063-6294a90a4340	2025-08-12	Warnings	Exact identifier application number: M017
Fast Freeze	MENTHOL	Natural Essentials Inc.	d8c42c8d-6ce0-43bf-b165-41979f3d8f79	2025-08-12	Warnings	Exact identifier application number: M017
Careland X-large Lidocaine 4 Pain Relieving	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	a6867506-4a46-47b1-b5b6-bfedb59dfde6	2025-08-11	Warnings	Exact identifier application number: M017
Dermedial Anti-Ouch	MENTHOL	Saje Natural Business Inc.	3c194b8f-cfa5-11e3-e063-6394a90a92de	2025-08-11	Warnings	Exact identifier application number: M017
Thera Plus Extra Strength Muscle Rub Topical Analgesic	MENTHOL	FOURSTAR GROUP USA, INC.	8a3b6adf-afbb-4d77-a19b-a6514ebd3b50	2025-08-11	Warnings	Exact identifier application number: M017
EARTHS CARE ARTHRITIS	CAPSAICIN	DLC Laboratories, Inc.	9460674b-057e-40b9-a0f9-ca3d92068d4f	2025-08-11	Warnings	Exact identifier application number: M017
LILAS PERIOD	MENTHOL	Lilas Wellness, Inc.	5ea53b4b-45e6-48a7-8090-09c3a21e7f63	2025-08-11	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Gel Roll-On	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	31639407-0f11-bde2-e063-6294a90af694	2025-08-10	Warnings	Exact identifier application number: M017
Chinese Red Tiger Lidocaine Patches	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	20cd369c-3e98-3d8f-e063-6394a90a0824	2025-08-10	Warnings	Exact identifier application number: M017
Treatonic LIDOCAINE PAIN RELIEF	LIDOCAINE 4%	100 KARMA INC	3bd66b03-ac82-2d45-e063-6294a90a610a	2025-08-08	Warnings	Exact identifier application number: M017
Capsaicin 0.025%	CAPSAICIN 0.025%	Advanced Rx of Tennessee, LLC	3bdcef94-d06f-9152-e063-6294a90a6072	2025-08-08	Warnings	Exact identifier application number: M017
MENTHOL 5%	MENTHOL 5%	Advanced Rx of Tennessee, LLC	3bdd0c52-29d8-ab67-e063-6294a90a9c45	2025-08-08	Warnings	Exact identifier application number: M017
Methyl Salicylate 25% Cream	METHYL SALICYLATE	Advanced Rx of Tennessee, LLC	3bdd3015-349a-0fac-e063-6394a90afe41	2025-08-08	Warnings	Exact identifier application number: M017
LIDOCAINE 4%	LIDOCAINE 4%	Advanced Rx of Tennessee, LLC	3bdd6b3d-7180-288c-e063-6394a90a1785	2025-08-08	Warnings	Exact identifier application number: M017
Good Sense Pain Relief Roll On	LIDOCAINE HCL	Geiss, Destin & Dunn, Inc	38e76fd6-e5fb-493c-e063-6294a90afed4	2025-08-08	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE
75IZZ8Y727	CAMPHOR OIL	8008-51-3	CAMPHOR OIL
UW86K581WY	CAPSICUM OLEORESIN	8023-77-6	CAPSICUM OLEORESIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
33346-3400-1	33346340001	1 VIAL, GLASS in 1 BOX (33346-3400-1) > 50 mL in 1 VIAL, GLASS (33346-3400-2)		2018-05-18	0000-00-00	No	No	Current
33346-3400-2	33346340002	50 mL in 1 VIAL, GLASS	50 ml					Historical
33346-3400-3	33346340003	50 mL in 1 BOTTLE	50 ml					Historical
33346-3400-4	33346340004	1 BOTTLE in 1 BOX (33346-3400-4) / 50 mL in 1 BOTTLE (33346-3400-3)	1 bottle	2024-11-24		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Relief+Recovery	Mayway Corporation	2025-12-23	HUMAN OTC DRUG LABEL	2
Relief+Recovery	Mayway Corporation	2020-12-31	HUMAN OTC DRUG LABEL	21