Home NDC 87841-937 Fit Mist Pain Relief
Product NDC 87841-937
11-digit product format 878410937
Labeler code 87841
Product ID 87841-937_56298fb7-59af-b9a3-e063-6294a90ac5e2
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form LIQUID
Route TOPICAL
Labeler Aroma Sensations Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-17
Substance MENTHOL
Active strength 44.9 mg/mL
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 Fit Mist Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 44.9 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 2747220 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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87841-937-00 87841093700 118 mL in 1 BOTTLE, SPRAY (87841-937-00) 118 ml 2026-06-17 No No Current 87841-937-01 87841093701 177 mL in 1 BOTTLE, SPRAY (87841-937-01) 177 ml 2026-07-02 No No Current