Home NDC 72835-202 Fenovar
Product NDC 72835-202
11-digit product format 728350202
Labeler code 72835
Product ID 72835-202_849d06ed-4398-4846-b597-8b5b85e8e1d8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Diclofenac Sodium and Menthol, Methyl salicylate
Dosage form KIT
Labeler V2 Pharma, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-01-21
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Fenovar
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311498 Internal RxNorm lookup 857700 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 51824-105-03 Fenovar 85 g in 1 TUBE CREAM 85 g 150 mg in 1g 7 65162-911-74 Fenovar 150 mL in 1 BOTTLE SOLUTION 150 mL 16.05 mg in 1mL 7 65162-911-74 Fenovar 1 in 1 CARTON SOLUTION 16.05 mg in 1mL 7 72835-202-02 Fenovar 1 in 1 CARTON KIT 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72835-202 FENOVAR (DICLOFENAC SODIUM AND MENTHOL, METHYL SALICYLATE) KIT [V2 PHARMA, LLC] 7 Current NDC, Legacy NDC, 4 package rows 20241103_cca25bd7-2afd-4ff1-adb3-0a77dfcd4342.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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Fenovar DICLOFENAC SODIUM AND MENTHOL, METHYL SALICYLATE V2 Pharma, LLC cca25bd7-2afd-4ff1-adb3-0a77dfcd4342 2024-11-01 Boxed warning, Warnings, Adverse reactions Exact identifier ndc (product): 72835-202
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51824-105-03 51824010503 85 g in 1 TUBE 85 g Historical 65162-911-74 65162091174 150 mL in 1 BOTTLE 150 ml Historical 72835-202-02 72835020202 1 KIT in 1 CARTON (72835-202-02) * 1 BOTTLE in 1 CARTON (65162-911-74) / 150 mL in 1 BOTTLE * 85 g in 1 TUBE (51824-105-03) 1 kit 2022-01-21 0000-00-00 No No Current