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 48 of 153 · 3,057 matching rows.
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