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 97 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AUVON Lidocaine Menthol Pain Relief Patch	LIDOCAINE AND MENTHOL	SHENZHEN YUWEN E-COMMERCE CO., LTD.	300cf469-5ca2-a40d-e063-6294a90a6801	2025-03-20	Warnings	Exact identifier application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15	CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONE	Carma Laboratories, Inc.	3a3af6e1-0281-462e-85e7-144cc5d46f32	2025-03-19	Warnings	Exact identifier application number: M017
Lidocaine 4%	LIDOCAINE	Innovida Pharmaeutique Corporation	eb83a3dd-557e-4334-b806-5fc05e9175a3	2025-03-19	Warnings	Exact identifier application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15	CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONE	Carma Laboratories, Inc.	c04059e9-8175-46c2-8582-f84ef193abd3	2025-03-19	Warnings	Exact identifier application number: M017
Carmex Variety Pack Classic Medicated Lip Balm Lip Balm SPF 15	CAMPHOR (SYNTHETIC), WHITE PETROLATUM, OCTINOXATE, OXYBENZONE	Carma Laboratories, Inc.	3a36a241-37a9-445a-a6e0-97709a7457a8	2025-03-19	Warnings	Exact identifier application number: M017
Herb Analgesic	HERB ANALGESIC PASTE	Changsha Maocheng Trading Co., Ltd	29373587-9eff-6ea0-e063-6394a90a23b2	2025-03-18	Warnings	Exact identifier application number: M017
DEBACHERE Butt Balm After Play Care Multi Symptoms Relief	BENZOCAINE, BENZALKONIUM CHLORIDE	DE.BACHERE USA LLC	f469b446-58a0-4be3-884f-d622b9d074f8	2025-03-17	Warnings	Exact identifier application number: M017
Auvon 4% Menthol Pain Relief Gel	MENTHOL	SHENZHEN YUWEN E-COMMERCE CO., LTD.	2dacd6fe-7d69-bcf0-e063-6294a90a0351	2025-03-14	Warnings	Exact identifier application number: M017
Eagle Medicated	MENTHOL METHYL SALICYLATE	Borden Company (Private) Limited	1ee49cad-84d4-42cf-aa83-c0da6f1b1b84	2025-03-14	Warnings	Exact identifier application number: M017
AY BENDITO THERMOACTIVE	MENTHOL, CAMPHOR	AY BENDITO INTERNATIONAL, INC	304d71b6-91c8-b2b6-e063-6394a90ab669	2025-03-14	Warnings	Exact identifier application number: M017
Hot/Cold Medicated Patch	HOT COLD PATCH	Dynarex	999881b3-287e-d975-e053-2995a90a87e3	2025-03-14	Warnings	Exact identifier application number: M017
Capsaicin 0.025%	CAPSAICIN 0.025%	Marcella Health	3054e7fd-cab2-7f77-e063-6294a90a498d	2025-03-14	Warnings	Exact identifier application number: M017
MENTHOL 5%	MENTHOL 5%	Marcella Health	30914c0a-fbda-5674-e063-6294a90aba5b	2025-03-14	Warnings	Exact identifier application number: M017
Peppermint Soothing Patch	CAMPHORIC ACID, MENTHOL, UNSPECIFIED FORM	Henan Lijitang Medical Technology Co., Ltd.	30361dd4-1f3d-ac5e-e063-6294a90a23bc	2025-03-13	Warnings	Exact identifier application number: M017
AVCOO Menthol Pain Relief Patch	MENTHOL	ADP Health Limited	3036804b-16c3-0c88-e063-6394a90a3084	2025-03-13	Warnings	Exact identifier application number: M017
LIDOCAINE 4%	LIDOCAINE 4%	Marcella Health	303d9462-cbfb-6251-e063-6394a90a7065	2025-03-13	Warnings	Exact identifier application number: M017
XeroBurn Burn Gel	LIDOCAINE HYDROCHLORIDE	Dynarex Corporation	58985046-ca9c-12be-e053-2991aa0abe72	2025-03-13	Warnings	Exact identifier application number: M017
Post Treatment Repair Cream	HYDROCORTISONE	Vege Labs LLC.	302d4327-354b-a252-e063-6394a90a20b6	2025-03-12	Warnings	Exact identifier application number: M017
TheraCare Pain Relief 4% Lidocaine	LIDOCAINE	Veridian Healthcare	2d3fc030-5d53-2acd-e063-6294a90a11ab	2025-03-11	Warnings	Exact identifier application number: M017
Cold Hot Medicated Patch 5% Menthol	MENTHOL	Veridian Healthcare	2d413707-794c-2fa8-e063-6394a90a06bf	2025-03-11	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