Home NDC 71101-985 HealthWise Cold Therapy Menthol Pain Relief
Product NDC 71101-985
11-digit product format 711010985
Labeler code 71101
Product ID 71101-985_484e86f3-c0d1-4327-e063-6294a90a3f27
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form SPRAY
Route TOPICAL
Labeler Veridian Healthcare
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-01
Substance MENTHOL
Active strength 10.5 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 HealthWise Cold Therapy Menthol Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10.5 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 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 71101-985-01 HealthWise Cold Therapy Menthol Pain Relief 90 mL in 1 BOTTLE SPRAY 90 1
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71101-985-01 71101098501 90 mL in 1 BOTTLE (71101-985-01) 90 ml 2026-01-13 No No Current