Home NDC 73240-905 Mineral Ice Methol Pain Relief
Product NDC 73240-905
11-digit product format 732400905
Labeler code 73240
Product ID 73240-905_55a126b3-450b-885a-e063-6394a90a39ca
Type HUMAN OTC DRUG
Nonproprietary name Menthol 10.5 %
Dosage form SPRAY
Route TOPICAL
Labeler Sunflora Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-12-01
Substance MENTHOL
Active strength 10.5 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 Mineral Ice Methol Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10.5 g/100g
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 1489073 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 108 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73240-905-01 73240090501 85 g in 1 CAN (73240-905-01) 85 g 2025-12-01 No No Current