PR

Product NDC: 72358-101
11-digit product format: 723580101
Labeler code: 72358
Product ID: 72358-101_4229f4ae-8934-0e10-e063-6394a90a4185
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol
Dosage form: LOTION
Route: TOPICAL
Labeler: Amphp, Inc
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-11-01
Substance: MENTHOL
Active strength: .5 g/100g
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 · 9 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
2025-02-02 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	72358-101-04	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72358-101-03	`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	72358-101-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72358-101-03	`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	72358-101-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72358-101-03	`0efc9e666f02…`	`f202fb6c5f17…`

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: PR
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.5 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
1293193	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
6f5b9e08-c445-4fac-e053-2a91aa0aa737	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72358-101-03	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-03-03	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-04	2025-01-30	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-02-14	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-01	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-02	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737
72358-101-03	2022-01-28	6f5b9e08-c445-4fac-e053-2a91aa0aa737

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72358-101-03	PR	20 g in 1 PACKET	LOTION	20		9
72358-101-04	PR	300 g in 1 BOTTLE, PLASTIC	LOTION	300		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72358-101	PR (MENTHOL) LOTION [AMPHP, INC]	8	Current NDC, Legacy NDC, 2 package rows	20250305_6f5b9e08-c445-4fac-e053-2a91aa0aa737.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 6 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Blaster Pain Relief Stick	MENTHOL, METHYL SALICYLATE, CAMPHOR	Kalahari Rose, LLC	587d660a-5f80-de5a-e063-6394a90aa287	2026-08-07	Warnings	Exact identifier application number: M017
Itch Relief	DIPHENHYDRAMINE HCL, ZINC ACETATE	Cardinal Health, 110 dba Leader	3ed7b8a1-012f-459d-878c-813b93d4673c	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Gel Cooling Pain Relief	MENTHOL	The Kroger Co.	6fb0acc8-8dab-452c-b09e-de97306e1c32	2026-08-06	Warnings, Adverse reactions	Exact identifier application number: M017
Lidocaine Tattoo Wipe	LIDOCAINE HYDROCHLORIDE	MD Tattoo Company	369c1d16-597c-e1dc-e063-6394a90a3104	2026-08-06	Warnings	Exact identifier application number: M017
Non-proprietary name	HEADACHE PATCH	Nanjing 3H Medical Products Co.,Ltd.	586d73f1-0b0b-f596-e063-6394a90a4d57	2026-08-06	Warnings	Exact identifier application number: M017
Point Relief Coldspot Pain Relieving	MENTHOL	Fabrication Enterprises Inc	479fb728-4aeb-42e3-b238-f04255514baa	2026-08-05	Warnings	Exact identifier application number: M017
Dealmed Burn	LIDOCAINE	Dealmed Medical Supplies, LLC.	3b5f7ded-c275-4d7f-9fd4-539797d5507e	2026-08-05	Warnings	Exact identifier application number: M017
Lidocaine HCl	LIDOCAINE HCL	Topco Associates LLC	584e1f35-4d99-9c85-e063-6294a90ab3d0	2026-08-05	Warnings, Adverse reactions	Exact identifier application number: M017
Hempe HOT Muscle and Joint Gel	HEMPE	Healthcare International Research Limited	5854a80e-c92b-3ff5-e063-6294a90a2d05	2026-08-05	Warnings	Exact identifier application number: M017
Lidocaine Plantar Relief Roll-On	LIDOCAINE	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	585ccb4b-3bff-39b9-e063-6294a90a0e18	2026-08-05	Warnings	Exact identifier application number: M017
Green MARVEL PAIN RELIEF	MENTHOL, CAMPHOR, METHYL SALICYLATE	Miramar Cosmetics, Inc DBA Miramar Lab	9ff6e477-ef79-4a0c-9e21-8cae0e5d8810	2026-08-05	Warnings	Exact identifier application number: M017
tuiwaro LIDOCAINE Cream	LIDOCAINE CREAM	Guangzhou Jingliang Cosmetics Co., Ltd.	56e36592-a935-61d4-e063-6294a90a6e4c	2026-08-04	Warnings	Exact identifier application number: M017
Mineral Ice Extreme Menthol Pain Relief	MENTHOL	Carlin Consumer Health LLC	584f5c6e-3385-3221-e063-6294a90aabae	2026-08-04	Warnings	Exact identifier application number: M017
hydrocortisone	HYDROCORTISONE	Bryant Ranch Prepack	484fe5e4-a058-49c0-a382-c8fc3e20c3b2	2026-08-04	Warnings	Exact identifier application number: M017
procure	HYDROCORTISONE ACETATE	TWIN MED, LLC	2670c9c4-66ad-40e8-a08a-582b160de39d	2026-08-03	Warnings	Exact identifier application number: M017
Wini By Locsanity Advanced Formula Muscle Joint Relief Balm	METHYL SALICYLATE,CAMPHOR,MENTHOL	Locsanity LLC	5829b5d7-78d4-78a2-e063-6394a90a3dfc	2026-08-03	Warnings	Exact identifier application number: M017
Icy Hot Original Nighttime Recovery Pain Relief No Mess Roll On	MENTHOL	Chattem, Inc.	aa40c907-eeb5-4fda-b35e-439cbecc178c	2026-07-31	Warnings	Exact identifier application number: M017
Alphamale Delay Cream	BENZOCAINE	Prodigy Media Inc	53d682ee-0802-a16d-e063-6394a90aeee1	2026-07-31	Warnings	Exact identifier application number: M017
Pure Primal Delay Cream	BENZOCAINE	Prodigy Media Inc	57e9e894-c14f-d806-e063-6394a90ab8e5	2026-07-31	Warnings	Exact identifier application number: M017
Satohap	DL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE	Sato Pharmaceutical Co., Ltd.	df0e2b83-8f61-4ed8-bcc4-55e4ea782090	2026-07-31	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1293193	menthol 0.5 % Topical Lotion	PSN	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9
1293193	menthol 5 MG/ML Topical Lotion	SCD	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9
1293193	menthol 0.5 % Topical Lotion	SY	6f5b9e08-c445-4fac-e053-2a91aa0aa737	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72358-101-01	72358010101	300 g in 1 TUBE (72358-101-01)	300 g	2018-11-01	0000-00-00	No	No	Current
72358-101-02	72358010102	100 g in 1 TUBE (72358-101-02)	100 g	2018-11-01	0000-00-00	No	No	Current
72358-101-03	72358010103	20 g in 1 PACKET (72358-101-03)	20 g	2018-11-01	0000-00-00	No	No	Current
72358-101-04	72358010104	300 g in 1 BOTTLE, PLASTIC (72358-101-04)	300 g	2018-11-01	0000-00-00	No	No	Current

PR