Home NDC 76348-409 Dr. Canuso foot repair serum
Product NDC 76348-409
11-digit product format 763480409
Labeler code 76348
Product ID 76348-409_350b8fbb-d869-9503-e063-6394a90a9eb8
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate serum
Dosage form LOTION
Route TOPICAL
Labeler Renu Laboratories, LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-08-20
Substance TOLNAFTATE
Active strength .3 g/28g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 76348-409-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 76348-409-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 76348-409-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 76348-409-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76348-409-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76348-409-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76348-409-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Dr. Canuso foot repair serum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE .3 g/28g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 283693 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76348-409-02 Dr. Canuso foot repair serum 28 g in 1 BOTTLE, PUMP LOTION 28 17 76348-409-02 Dr. Canuso foot repair serum 1 in 1 BOX LOTION 1 17
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TOLNAFTATE ACTIVE INGREDIENT 06KB629TKV DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 TOLNAFTATE ACTIVE MOIETY 06KB629TKV DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 2-HYDROXYETHYL ACRYLATE INACTIVE INGREDIENT 25GT92NY0C DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 ACETYLATED LANOLIN ALCOHOLS INACTIVE INGREDIENT SNN716810P DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 BENZOIC ACID INACTIVE INGREDIENT 8SKN0B0MIM DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 CETYL ACETATE INACTIVE INGREDIENT 4Q43814HXS DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 CYCLOMETHICONE 5 INACTIVE INGREDIENT 0THT5PCI0R DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 DEHYDROACETIC ACID INACTIVE INGREDIENT 2KAG279R6R DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 DIETHYLENE GLYCOL MONOETHYL ETHER INACTIVE INGREDIENT A1A1I8X02B DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 MENTHOL INACTIVE INGREDIENT L7T10EIP3A DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 MENTHYL LACTATE, (-)- INACTIVE INGREDIENT 2BF9E65L7I DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 OLIVE OIL INACTIVE INGREDIENT 6UYK2W1W1E DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 PEG-12 DIMETHICONE (300 CST) INACTIVE INGREDIENT ZEL54N6W95 DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 PHENOXYETHANOL INACTIVE INGREDIENT HIE492ZZ3T DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 PHENYL TRIMETHICONE INACTIVE INGREDIENT DR0K5NOJ4R DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 POLYSORBATE 60 INACTIVE INGREDIENT CAL22UVI4M DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 SODIUM ACRYLOYLDIMETHYLTAURATE INACTIVE INGREDIENT 2T9Q6EKI0G DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 SQUALANE INACTIVE INGREDIENT GW89575KF9 DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 TALC INACTIVE INGREDIENT 7SEV7J4R1U DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13 WATER INACTIVE INGREDIENT 059QF0KO0R DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, INC.] 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76348-409 DR. CANUSO FOOT REPAIR SERUM (TOLNAFTATE SERUM) LOTION [RENU LABORATORIES, LLC] 17 Current NDC, Legacy NDC, 2 package rows 20250515_1fcc52c5-7030-13cb-e054-00144ff8d46c.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 22 of 51 · 1,004 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Jock Itch Clotrimazole Antifungal CLOTRIMAZOLE WalMart a7677ad4-5239-40da-809a-501b91caedbf 2026-01-29 Warnings Exact identifier application number: M005 ProCure Antifungal MICONAZOLE NITRATE 2% Twin Med LLC 3d380fe4-a870-cb55-e063-6394a90a9c90 2026-01-28 Warnings Exact identifier application number: M005 Antifungal Liquid TOLNAFTATE Wal-Mart Stores, Inc. 401f4993-0200-f1fd-e063-6294a90a6589 2026-01-28 Warnings Exact identifier application number: M005 Foot Powder MICONAZOLE NITRATE Walgreens Company 137a493b-6ed5-d649-e063-6294a90ac442 2026-01-28 Warnings Exact identifier application number: M005 Miconazole Nitrate JOCK ITCH SPRAY Wal-Mart Stores, Inc. 76259769-9923-4856-a160-a738bc8a72f0 2026-01-27 Warnings Exact identifier application number: M005 Signature Select Instant Hand Sanitizer Wipes with Aloe Vera ALCOHOL Living Better Brands LLC cf4b671f-697a-47d3-921e-2de433073918 2026-01-26 Warnings Exact identifier application number: M005 Signature Select Advanced Hand Sanitizer with Aloe Vera ALCOHOL Living Better Brands LLC cbf0fead-0729-460b-82c0-1596c995cf2b 2026-01-26 Warnings Exact identifier application number: M005 Signature Select Advanced Hand Sanitizer ALCOHOL Living Better Brands LLC 6d1cc25b-d612-4aae-bdb0-304758ef8f0f 2026-01-26 Warnings Exact identifier application number: M005 clotrimazole CLOTRIMAZOLE Padagis Israel Pharmaceuticals Ltd 3dcd0158-ec51-4fa7-a26a-02c2926156c0 2026-01-22 Warnings Exact identifier application number: M005 Puriya Antifungal Balm ZINC UNDECYLENATE IPC Republic, Inc. 96bf44bc-b5eb-4198-9056-02e51665a162 2026-01-22 Warnings Exact identifier application number: M005 BZK Antiseptic BENZALKONIUM CHLORIDE Lights Medical Manufacture Co., Ltd. 698ed472-9204-46e3-95a4-d59e204628ac 2026-01-21 Warnings Exact identifier application number: M005 LIGHTS Swabstick BENZALKONIUM CHLORIDE Lights Medical Manufacture Co., Ltd. 9346512e-53a1-420a-8b4d-bfbec32576a2 2026-01-21 Warnings Exact identifier application number: M005 Lights Isopropyl Alcohol Prep Pads ISOPROPYL ALCOHOL Lights Medical Manufacture Co., Ltd. 4905a27c-6cf8-4b1a-a02c-4c81756e8c0a 2026-01-21 Warnings Exact identifier application number: M005 Bee Venom Fungal Nail Treatment Liquid BEE VENOM FUNGAL NAIL TREATMENT Shenzhen Earth Surface Trading Co., Ltd. 48d164bc-dab6-6fe4-e063-6394a90a3fc4 2026-01-20 Warnings Exact identifier application number: M005 Tolnaftate MEIJER ATHLETES FOOT LIQUID SPRAY Meijer Distribution Inc. d9f7753f-aef9-86e2-e053-2995a90a2082 2026-01-20 Warnings Exact identifier application number: M005 Tolnaftate FOOT ODOR CONTROL POWDER SPRAY Meijer Distribution Inc b3ba676e-9377-4665-b99e-d4143df96b36 2026-01-20 Warnings Exact identifier application number: M005 Tolnaftate MEIJER ATHLETES FOOT LIQUID Meijer Distribution Inc. 0399dfef-9ea6-6fe4-e063-6394a90aec43 2026-01-20 Warnings Exact identifier application number: M005 TOENAIL FUNGUS TREATMENT MAXIMUM STRENGTH Liquid TOLNAFTATE Shenzhen Ctrip Technology Co., Ltd. 1fb03184-5f21-c82a-e063-6294a90a9fa4 2026-01-19 Warnings Exact identifier application number: M005 Miconazole Nitrate MICONAZOLE NITRATE AvKARE 1a26534d-eeb8-8d17-e063-6294a90a70c7 2026-01-19 Warnings Exact identifier application number: M005 Hermon Antifungal Soap. 4 packs TOLNAFTATE 1% Beautivity LLC 42c769de-f1e1-b3a1-e063-6394a90ab2a1 2026-01-18 Warnings Exact identifier application number: M005
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 76348-409-02 76348040902 1 BOTTLE, PUMP in 1 BOX (76348-409-02) / 28 g in 1 BOTTLE, PUMP 2015-08-20 0000-00-00 No No Current