Auvon 4% Menthol Pain Relief Gel

Product NDC: 83391-007
11-digit product format: 833910007
Labeler code: 83391
Product ID: 83391-007_30497f20-958d-044a-e063-6294a90a0b07
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: GEL
Route: TOPICAL
Labeler: SHENZHEN YUWEN E-COMMERCE CO., LTD.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-02-08
Substance: LEVOMENTHOL
Active strength: .04 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Auvon 4% Menthol Pain Relief Gel
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LEVOMENTHOL	.04 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
BZ1R15MTK7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
415974	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
2dacd6fe-7d69-bcf0-e063-6294a90a0351	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
83391-007-01	Auvon 4% Menthol Pain Relief Gel	89 mL in 1 BOTTLE	GEL	89	4
83391-007-02	Auvon 4% Menthol Pain Relief Gel	2 in 1 PACKAGE	GEL	2	4
83391-007-03	Auvon 4% Menthol Pain Relief Gel	3 in 1 PACKAGE	GEL	3	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83391-007	AUVON 4% MENTHOL PAIN RELIEF GEL (MENTHOL) GEL [SHENZHEN YUWEN E-COMMERCE CO., LTD.]	4	Current NDC, 3 package rows	20250316_2dacd6fe-7d69-bcf0-e063-6294a90a0351.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 151 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
EXOTEN-C	METHYL SALICYLATE, MENTHOL, CAPSAICIN	Asclemed USA, Inc.	76ed37e0-64b5-4abe-a03c-3dc7084a3919	2023-10-16	Warnings	Exact identifier application number: M017
Calypxo Pain Relief	METHYL SALICYLATE, MENTHOL	Asclemed USA, Inc	bd9d0bc0-5705-4c73-bcd6-f6cdb68e05b6	2023-10-16	Warnings	Exact identifier application number: M017
Calypxo HP Pain Relief	METHYL SALICYLATE, MENTHOL	Asclemed USA, Inc	89a8c267-bd92-4d0d-8e50-c52224aff9cd	2023-10-16	Warnings	Exact identifier application number: M017
Zylotrol	LIDOCAINE HCL 4%, MENTHOL 1%	Whitestone Products LLC	0e32e9c0-ff5b-4e88-89b1-f5903cd98209	2023-10-16	Warnings	Exact identifier application number: M017
Capsadyn	CAPSAICIN	Chorda Pharma, Inc	07731045-0d2b-76b7-e063-6294a90af921	2023-10-11	Warnings	Exact identifier application number: M017
WHITE FLOWER STRAIN RELIEF	CAMPHOR, MENTHOL AND METHYL SALICYLATE	HOE HIN PAK FAH YEOW MANUFACTORY LTD	65282267-de63-453a-a686-f8752c71b9ef	2023-10-02	Warnings	Exact identifier application number: M017
WHITE FLOWER ANALGESIC BALM FLORAL SCENTED	CAMPHOR, MENTHOL AND METHYL SALICYLATE	HOE HIN PAK FAH YEOW MANUFACTORY LTD	4e9cb5aa-b0aa-4a5c-b561-cc38437758d8	2023-10-02	Warnings	Exact identifier application number: M017
NATUREANCE BODY BALM	CAMPHOR	EROS GLOBAL CORP	05b84fd2-8d8f-9249-e063-6294a90ae29f	2023-09-19	Warnings	Exact identifier application number: M017
U ICE COLD	MENTHOL	UNIVERSAL DISTRIBUTION CENTER LLC	752ef0cd-f12a-3b9e-e053-2991aa0abeb1	2023-09-01	Warnings	Exact identifier application number: M017
Family Wellness Pain Relief with Lidocaine	PAIN RELIEF WITH LIDOCAINE	FAMILY DOLLAR (Family Wellness)	3a18119f-6c75-4cea-a990-97cb8a9589d4	2023-08-29	Warnings	Exact identifier application number: M017
Bactine Max Antibiotic and Lidocaine Max Pain Relief	LIDOCAINE	WellSpring Pharmaceutical Corporation	71300df9-6113-4f25-93ca-28ad7e7f79de	2023-06-08	Warnings	Exact identifier application number: M017
Bactine Max Lidocaine Roll-on 2.5oz	LIDOCAINE	WellSpring Pharmaceutical Corporation	09b32a98-9131-451e-87a6-81a1e4ed7ec5	2023-04-25	Warnings	Exact identifier application number: M017
Icy Hot Pro Dry	CAMPHOR, MENTHOL	Chattem, Inc.	4de1bc29-d166-4599-9e75-5f841bf20967	2023-03-01	Warnings	Exact identifier application number: M017
Icy Hot Vanishing Scent	MENTHOL	Chattem, Inc.	e2092016-9741-433d-92e6-74bfddadb72c	2022-09-29	Warnings	Exact identifier application number: M017
New Terocin	METHYL SALICYLATE, CAPSAICIN, AND MENTHOL	Alexso, Inc	5dbd5fc0-a27e-4979-aca7-28f73096fd5f	2022-08-18	Warnings	Exact identifier application number: M017
FIRSTAR Sting Relief Pad	BENZOCAINE	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	0e491a7a-4204-439f-862d-741cbc0be9fd	2021-07-06	Warnings	Exact identifier application number: M017
Arthritis Relief GoodSense	TROLAMINE SALICYLATE	Geiss, Destin & Dunn, Inc	a253730a-2187-07de-e053-2a95a90a9877	2020-04-02	Warnings	Exact identifier application number: M017
Aloe Cort	HYDROCORTISONE	Topiderm, Inc.	789a6669-3320-4558-8d6f-ab255db50d8d	2019-09-17	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Roll On Refresh	CAMPHOR, MENTHOL	Borden Company (Private) Limited	567b6820-fb52-630e-e063-6294a90a8bf8	2015-07-01	Warnings	Exact identifier application number: M017
Eagle Brand Medicated Oil Aromatic	CAMPHOR, MENTHOL, METHYL SALICYLATE	Borden Company (Private) Limited	54e45d89-e8c3-6fc3-e063-6394a90aac4e	2015-06-15	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
BZ1R15MTK7	LEVOMENTHOL	2216-51-5	LEVOMENTHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
415974	menthol 4 % Topical Gel	PSN	2dacd6fe-7d69-bcf0-e063-6294a90a0351	4
415974	menthol 0.04 MG/MG Topical Gel	SCD	2dacd6fe-7d69-bcf0-e063-6294a90a0351	4
415974	menthol 4 % Topical Gel	SY	2dacd6fe-7d69-bcf0-e063-6294a90a0351	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
83391-007-01	83391000701	89 mL in 1 BOTTLE (83391-007-01)	89 ml	2025-02-08	No	No	Current
83391-007-02	83391000702	2 BOTTLE in 1 PACKAGE (83391-007-02) / 89 mL in 1 BOTTLE (83391-007-01)	2 bottle	2025-02-08	No	No	Current
83391-007-03	83391000703	3 BOTTLE in 1 PACKAGE (83391-007-03) / 89 mL in 1 BOTTLE (83391-007-01)	3 bottle	2025-02-08	No	No	Current