QR PAIN

Product NDC: 73180-075
Requested package NDC: 73180-075-01
11-digit product format: 731800075
Labeler code: 73180
Product ID: 73180-075_439705ff-9d40-ae69-e063-6394a90a58eb
Type: HUMAN OTC DRUG
Nonproprietary name: Analgesic
Dosage form: CREAM
Route: TOPICAL
Labeler: MARYHELENE ENTERPRISES INC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-08-01
Substance: MANNITOL; MENTHOL
Active strength: 30; 1.25 g/100g; g/100g
Pharmacologic classes: Increased Diuresis [PE], Osmotic Activity [MoA], Osmotic Diuretic [EPC]
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	73180-075	73180-075-01	D	Discontinued by firm		2026-10-23

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: QR PAIN
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MANNITOL	30 g/100g
MENTHOL	1.25 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3OWL53L36A	Internal UNII lookup
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
2182800	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
9984a510-30be-4013-e053-2995a90a841e	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73180-075-00	QR PAIN	75 g in 1 TUBE	CREAM	75		7
73180-075-01	QR PAIN	1 in 1 BOX	CREAM	1		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73180-075	QR PAIN (ANALGESIC) CREAM [MARYHELENE ENTERPRISES INC]	6	Current NDC, Legacy NDC, 2 package rows	20250119_9984a510-30be-4013-e053-2995a90a841e.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 118 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tiger Balm	METHYL SALICYLATE AND MENTHOL	Haw Par Healthcare Ltd.	51293a06-5922-4072-ae14-afaba9c1b58e	2024-11-14	Warnings	Exact identifier application number: M017
Tylenol Precise Warming Pain Relieving	LIDOCAINE	Kenvue Brands LLC	0c60b607-ade9-68f2-e063-6394a90a4025	2024-11-13	Warnings	Exact identifier application number: M017
Tylenol Precise Pain Relieving	LIDOCAINE	Kenvue Brands LLC	fc1e0451-8c84-729e-e053-6394a90aaba0	2024-11-13	Warnings	Exact identifier application number: M017
Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving	NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	23222e54-d793-4d79-980e-550e32a95742	2024-11-13	Warnings	Exact identifier application number: M017
TopCare Pain Relieving Roll-On Topical Analgesic	MENTHOL, UNSPECIFIED FORM	Topco Associates LLC	48589893-ca67-471d-88bc-92014295ab9f	2024-11-13	Warnings	Exact identifier application number: M017
Benadryl Extra Strength Itch Stopping	DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE	Kenvue Brands LLC	a1c1b878-d58f-41ff-b7a8-477f28c52667	2024-11-12	Warnings	Exact identifier application number: M017
Real Time Pain Relief Maxx Plus Topical Analgesic	MENTHOL	Real Time Products Inc.	fc509a55-594d-4d44-87db-33286e937581	2024-11-12	Warnings	Exact identifier application number: M017
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	Acme United Corporation	f1f051ad-7e82-9d1a-e053-2a95a90ac7d3	2024-11-12	Warnings	Exact identifier application number: M017
HYDROCORTISONE	HYDROCORTISONE	ALLIED TRADE LINK LLC	26bc238d-3bda-0c29-e063-6394a90a35fb	2024-11-12	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Acme United Corporation	fabcaa3b-d189-bd29-e053-6294a90ae86b	2024-11-12	Warnings	Exact identifier application number: M017
ActivICE	MENTHOL	Medline Industries, LP	8414aea2-52b5-4221-e053-2a91aa0a622e	2024-11-12	Warnings	Exact identifier application number: M017
Pain Relieving Gel-Patch	LIDOCAINE	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	26c7116f-c86d-8752-e063-6294a90ab73f	2024-11-12	Warnings	Exact identifier application number: M017
Hydrocortisone	HYDROCORTISONE	Kroger Company	fc1677f2-4078-4ebd-9c3b-86a29a35b489	2024-11-12	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Cream	LIDOCAINE	CVS Health	ad950680-c03c-4fa5-aa7f-239a889cd097	2024-11-12	Warnings	Exact identifier application number: M017
CVS Arthritis Pain Relief	ARTHRITIS PAIN RELIEF	CVS Health	575dd514-fd99-4e44-8fc8-52938f9abc26	2024-11-11	Warnings	Exact identifier application number: M017
ThermaPatch (TM) Lidocaine Pain Relief Patch	LIDOCAINE PAIN RELIEF PATCH	Henan Enokon Medical Instrument Co., Ltd.	26769590-cd50-1b01-e063-6394a90a445c	2024-11-09	Warnings	Exact identifier application number: M017
DG Health Cold Zone Pain Relieving Topical Analgesic	MENTHOL, UNSPECIFIED FORM	Dolgencorp Inc	22594ab8-9a4a-426f-aced-5c636620fa2c	2024-11-08	Warnings	Exact identifier application number: M017
Peviderm Pramoxine Hydrocholride 1%	PRAMOXINE HYDROCHLORIDE	Stratus Pharmaceuticals Inc	680b40fa-1922-443a-a4b0-7c3f6a2b847d	2024-11-07	Warnings	Exact identifier application number: M017
Meijer Analgesic with Aloe Topical Analgesic	TROLAMINE SALICYLATE	Meijer Distribution, Inc	f6c1e09e-4c61-4c2a-87d7-b052ed36fcac	2024-11-07	Warnings	Exact identifier application number: M017
Meijer Pain Relieving Balm Analgesic	TROLAMINE SALICYLATE	Meijer Distribution, Inc	1b7535cc-01ac-49f0-9889-dd14b254d4ae	2024-11-07	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3OWL53L36A	MANNITOL	69-65-8	MANNITOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2182800	mannitol 30 % / menthol 1.25 % Topical Cream	PSN	9984a510-30be-4013-e053-2995a90a841e	7
2182800	mannitol 300 MG/ML / menthol 12.5 MG/ML Topical Cream	SCD	9984a510-30be-4013-e053-2995a90a841e	7
2182800	mannitol 30 % / menthol 1.25 % Topical Cream	SY	9984a510-30be-4013-e053-2995a90a841e	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
73180-075-01	73180007501	1 TUBE in 1 BOX (73180-075-01) / 75 g in 1 TUBE (73180-075-00)	1 tube	2019-08-01	0000-00-00	No	No	Current