Home NDC 83391-003 AUVON Pain Relief Roll-on
Product NDC 83391-003
11-digit product format 833910003
Labeler code 83391
Product ID 83391-003_28c451bc-3a8b-ae1d-e063-6294a90ad61c
Type HUMAN OTC DRUG
Nonproprietary name menthol
Dosage form SOLUTION
Route TOPICAL
Labeler SHENZHEN YUWEN E-COMMERCE CO., LTD.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-09-21
Substance MENTHOL
Active strength 4 g/100mL
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 Pain Relief Roll-on
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 4 g/100mL
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 283438 Internal RxNorm 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 83391-003-01 AUVON Pain Relief Roll-on 1 in 1 PACKAGE SOLUTION 1 2 83391-003-01 AUVON Pain Relief Roll-on 74 mL in 1 BOTTLE SOLUTION 74 2 83391-003-02 AUVON Pain Relief Roll-on 2 in 1 PACKAGE SOLUTION 2 2 83391-003-02 AUVON Pain Relief Roll-on 74 mL in 1 BOTTLE SOLUTION 74 2 83391-003-03 AUVON Pain Relief Roll-on 74 mL in 1 BOTTLE SOLUTION 74 2 83391-003-03 AUVON Pain Relief Roll-on 3 in 1 PACKAGE SOLUTION 3 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83391-003 AUVON PAIN RELIEF ROLL-ON (MENTHOL) SOLUTION [SHENZHEN YUWEN E-COMMERCE CO., LTD.] 2 Current NDC, 6 package rows 20241209_df239c4d-af6a-41ca-baed-d0788782ce9f.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 110 of 153 · 3,057 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 83391-003-01 83391000301 1 BOTTLE in 1 PACKAGE (83391-003-01) / 74 mL in 1 BOTTLE 1 bottle 2024-09-21 No No Current 83391-003-02 83391000302 2 BOTTLE in 1 PACKAGE (83391-003-02) / 74 mL in 1 BOTTLE 2 bottle 2024-09-21 No No Current 83391-003-03 83391000303 3 BOTTLE in 1 PACKAGE (83391-003-03) / 74 mL in 1 BOTTLE 3 bottle 2024-09-21 No No Current