Home NDC 71101-090 TheraCare Roll-on Menthol 4% Pain Relief
Product NDC 71101-090
11-digit product format 711010090
Labeler code 71101
Product ID 71101-090_3f694987-bd01-d332-e063-6294a90a5b1f
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler Veridian Healthcare
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-01
Substance MENTHOL
Active strength 4 g/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 TheraCare Roll-on Menthol 4% Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 4 g/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 71101-090-01 TheraCare Roll-on Menthol 4% Pain Relief 73 mL in 1 BOTTLE, WITH APPLICATOR GEL 73 1 71101-090-01 TheraCare Roll-on Menthol 4% Pain Relief 1 in 1 CARTON GEL 1 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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 71101-090-01 71101009001 1 BOTTLE, WITH APPLICATOR in 1 CARTON (71101-090-01) / 73 mL in 1 BOTTLE, WITH APPLICATOR 2025-09-01 No No Current