Home NDC 41250-350 Meijer Maximum Strength Pain Relieving
Product NDC 41250-350
11-digit product format 412500350
Labeler code 41250
Product ID 41250-350_2c052527-8626-4799-8c2c-1ebaa310890c
Type HUMAN OTC DRUG
Nonproprietary name menthol, unspecified form
Dosage form LIQUID
Route TOPICAL
Labeler Meijer Distribution, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-02-24
Substance MENTHOL, UNSPECIFIED FORM
Active strength 160 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 Meijer Maximum Strength Pain Relieving
Brand name suffix Analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 160 mg/mL
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 866084 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-350-01 Meijer Maximum Strength Pain RelievingAnalgesic 1 in 1 CARTON LIQUID 1 4 41250-350-01 Meijer Maximum Strength Pain RelievingAnalgesic 74 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 74 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-350 MEIJER MAXIMUM STRENGTH PAIN RELIEVING ANALGESIC (MENTHOL, UNSPECIFIED FORM) LIQUID [MEIJER DISTRIBUTION, INC] 3 Current NDC, Legacy NDC, 2 package rows 20241108_bd6f04f9-a23b-45f6-bce2-1ef7203198e1.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 152 · 3,029 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lidocaine LIDOCAINE Patrin Pharma Inc. 91eedf9d-53b8-49d5-af59-25019606a0b2 2024-11-15 Warnings Exact identifier application number: M017 equaline anti itch maximum strength HYDROCORTISONE United Natural Foods, Inc. dba UNFI d1ac686e-62f2-4177-8abc-8c7ca578de1a 2024-11-15 Warnings Exact identifier application number: M017 Meijer Pain Relieving Max Strength with Lavender Essential Oil Analgesic LIDOCAINE HYDROCHLORIDE Meijer Distribution, Inc e688967e-799a-4fc8-a19a-f0012b90e76b 2024-11-15 Warnings Exact identifier application number: M017 basic care hydrocortisone HYDROCORTISONE Amazon.com Services LLC a0d0e82b-03ff-4d43-9be0-0e414ee49970 2024-11-15 Warnings Exact identifier application number: M017 DG health hydrocortisone HYDROCORTISONE Dolgencorp, LLC 40710bae-32bb-47fd-b3dd-31d2c98ee70f 2024-11-15 Warnings Exact identifier application number: M017 Meijer Ultra Strength Pain Relieving Topical Analgesic CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE Meijer Distribution, Inc 6319b019-8e17-4de1-b4e0-b402288a97d4 2024-11-15 Warnings Exact identifier application number: M017 Meijer Pain Relieving analgesic CAMPHOR (SYNTHETIC) AND MENTHOL, UNSPECIFIED FORM Meijer Distribution, Inc 9953be94-5768-448f-83de-f5e53a2972cc 2024-11-15 Warnings Exact identifier application number: M017 careone anti itch HYDROCORTISONE American Sales Company 5f7b1435-ebee-4093-847a-79e8d6641404 2024-11-15 Warnings Exact identifier application number: M017 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
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 41250-350-01 41250035001 1 BOTTLE, WITH APPLICATOR in 1 CARTON (41250-350-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR 2019-02-24 0000-00-00 No No Current