Home NDC 73180-075 QR PAIN
Product NDC 73180-075
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 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 · 24 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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 73180-075-01 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.
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 122 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sanar Naturals Arnica Reforzada CAMPHOR Sanvall Enterprises, Inc 1921a4b1-cd36-195e-e063-6294a90a8793 2024-10-31 Warnings Exact identifier application number: M017 Sanar Naturals Arnica Pain Releiving Roll On with Camphor CAMPHOR Sanvall Enterprises, Inc 173db0e2-611f-55b9-e063-6394a90ac987 2024-10-31 Warnings Exact identifier application number: M017 Sanar Naturals Camphor CAMPHOR Sanvall Enterprises, Inc 1921e851-cf83-0bdb-e063-6294a90a357f 2024-10-31 Warnings Exact identifier application number: M017 cortisone HYDROCORTISONE CVS Pharmacy c766deac-d993-4e48-a5c3-4cfde7338dff 2024-10-31 Warnings Exact identifier application number: M017 Walgreens Pain Relieving with Lavender Analgesic LIDOCAINE HYDROCHLORIDE Walgreen Company 6c7b39c8-5b65-430a-a529-5b6b14adce18 2024-10-31 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Plus Turmeric Analgesic TROLAMINE SALICYLATE Walgreen Company f3a121bc-7572-49a4-9822-2b6d858c19d2 2024-10-31 Warnings Exact identifier application number: M017 dg health hydrocortisone HYDROCORTISONE Dolgencorp, LLC 27dc9e09-fc4f-4b66-a303-177725f3a513 2024-10-31 Warnings Exact identifier application number: M017 basic care hydrocortisone HYDROCORTISONE Amazon.com Services LLC f5419859-3f9f-43ff-9a3f-6aa81af044f0 2024-10-31 Warnings Exact identifier application number: M017 ARCTIC RELIEF MENTHOL, UNSPECIFIED FORM STRATUS PHARMACEUTICALS INC d27fbc17-46b7-4d52-ba29-c99b6c63144a 2024-10-31 Warnings Exact identifier application number: M017 Pain Relief Gel-Patch LIDOCAINE, MENTHOL R & Y Group, LLC fe0478d8-2f06-cd56-e053-6294a90a58e5 2024-10-30 Warnings Exact identifier application number: M017 JOINT-RITIS PAIN RELIEVING ROLL-ON MENTHOL Lifeline Naturals of America, Inc. ec5d99c4-6bba-45d1-84e0-12fb7cb31495 2024-10-30 Warnings Exact identifier application number: M017 Walgreens Pain Relieving with Turmeric Analgesic LIDOCAINE HYDROCHLORIDE Walgreen Company 317ec4fb-cff0-461d-9ca0-299527a3686d 2024-10-30 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Analgesic CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE Walgreen Company 3215a676-104c-43c3-aa36-b30d5b67799a 2024-10-30 Warnings Exact identifier application number: M017 Ultra-Strength Pain Relief Analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM TARGET CORPORATION 159c5a84-bf68-41dd-a2d3-bc2402037244 2024-10-30 Warnings Exact identifier application number: M017 DG Health Cold n Hot Pain Relieving Topical Analgesic MENTHOL, UNSPECIFIED FORM Dolgencorp Inc 8fe13b85-ab74-42f8-a664-d3d2959921ac 2024-10-30 Warnings Exact identifier application number: M017 DEBACHERE Butt Balm After Care Antiseptic Pain Relief BENZOCAINE, BENZALKONIUM CHLORIDE DE.BACHERE USA LLC 8ba42864-69bf-455c-98d4-7f4ff94edceb 2024-10-29 Warnings Exact identifier application number: M017 Signature Care Hydrocortisone HYDROCORTISONE Safeway beefab66-b056-4bf1-b047-0780704ab87e 2024-10-29 Warnings Exact identifier application number: M017 Hydrocortisone HYDROCORTISONE H E B 15eb4676-5f6e-4c28-b5b9-4e45412dc37a 2024-10-29 Warnings Exact identifier application number: M017 Rael PAIN RELIEF ROLL-ON Analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM Rael, Inc. e6c49606-7c13-4dc6-a22d-ba54173ba788 2024-10-28 Warnings Exact identifier application number: M017 Monistat Care Instant Itch Relief BENZOCAINE Insight Pharmaceuticals LLC 4e9dc791-419f-4c79-aed4-760f8c17a5dd 2024-10-25 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 73180-075-00 73180007500 75 g in 1 TUBE 75 g Historical 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