Home NDC 83391-007 Auvon 4% Menthol Pain Relief Gel
Product NDC 83391-007
11-digit product format 833910007
Labeler code 83391
Product ID 83391-007_30497f20-958d-044a-e063-6294a90a0b07
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler SHENZHEN YUWEN E-COMMERCE CO., LTD.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-08
Substance LEVOMENTHOL
Active strength .04 mg/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 Auvon 4% Menthol Pain Relief Gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEVOMENTHOL .04 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BZ1R15MTK7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 415974 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83391-007-01 Auvon 4% Menthol Pain Relief Gel 89 mL in 1 BOTTLE GEL 89 4 83391-007-02 Auvon 4% Menthol Pain Relief Gel 2 in 1 PACKAGE GEL 2 4 83391-007-03 Auvon 4% Menthol Pain Relief Gel 3 in 1 PACKAGE GEL 3 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83391-007 AUVON 4% MENTHOL PAIN RELIEF GEL (MENTHOL) GEL [SHENZHEN YUWEN E-COMMERCE CO., LTD.] 4 Current NDC, 3 package rows 20250316_2dacd6fe-7d69-bcf0-e063-6294a90a0351.zip
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 109 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83391-007-01 83391000701 89 mL in 1 BOTTLE (83391-007-01) 89 ml 2025-02-08 No No Current 83391-007-02 83391000702 2 BOTTLE in 1 PACKAGE (83391-007-02) / 89 mL in 1 BOTTLE (83391-007-01) 2 bottle 2025-02-08 No No Current 83391-007-03 83391000703 3 BOTTLE in 1 PACKAGE (83391-007-03) / 89 mL in 1 BOTTLE (83391-007-01) 3 bottle 2025-02-08 No No Current