Home NDC 76176-239 NUVALU ICE THERAPY MENTHOL PAIN RELIEVING
Product NDC 76176-239
11-digit product format 761760239
Labeler code 76176
Product ID 76176-239_5ae0032c-b253-2e62-e063-6294a90afb96
Type HUMAN OTC DRUG
Nonproprietary name menthol
Dosage form GEL
Route TOPICAL
Labeler NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
Substance MENTHOL
Active strength 1.25 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 NUVALU ICE THERAPY MENTHOL PAIN RELIEVING
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 1.25 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 866128 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 8 of 156 · 3,115 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76176-239-24 76176023924 227 g in 1 JAR (76176-239-24) 227 g 2026-01-01 No No Current