Home NDC 76348-401 Molecular AF
Product NDC 76348-401
11-digit product format 763480401
Labeler code 76348
Product ID 76348-401_2d3f2f5e-be56-71e9-e063-6294a90a6ac2
Type HUMAN OTC DRUG
Nonproprietary name tolnaftate
Dosage form OIL
Route TOPICAL
Labeler Renu Laboratories, LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-07-01
Substance TOLNAFTATE
Active strength .01 mg/mL
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 · 27 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 2025-02-02 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 76348-401-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 76348-401-01 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 76348-401-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 76348-401-01 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 76348-401-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 76348-401-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 76348-401-02 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 76348-401-01 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 76348-401-02 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 76348-401-01 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 76348-401-02 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 76348-401-01 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 76348-401-02 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 76348-401-01 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 76348-401-02 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 76348-401-01 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 76348-401-02 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 76348-401-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
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 Molecular AF
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE .01 mg/mL
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1362937 Internal RxNorm lookup 1362942 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 76348-401-01 Molecular AF 11.5 mL in 1 BOTTLE OIL 11.5 4 76348-401-02 Molecular AF 11.5 mL in 1 BOX OIL 11.5 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TOLNAFTATE ACTIVE INGREDIENT 06KB629TKV MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 TOLNAFTATE ACTIVE MOIETY 06KB629TKV MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 CINNAMON OIL INACTIVE INGREDIENT E5GY4I6YCZ MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 CITRIC ACID MONOHYDRATE INACTIVE INGREDIENT 2968PHW8QP MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 DIETHYLENE GLYCOL MONOETHYL ETHER INACTIVE INGREDIENT A1A1I8X02B MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 ETHYL MACADAMIATE INACTIVE INGREDIENT ANA2NCS6V1 MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 OLIVE OIL INACTIVE INGREDIENT 6UYK2W1W1E MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 POTASSIUM SORBATE INACTIVE INGREDIENT 1VPU26JZZ4 MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2 TEA TREE OIL INACTIVE INGREDIENT VIF565UC2G MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76348-401 MOLECULAR AF (TOLNAFTATE) OIL [RENU LABORATORIES, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20250206_1b47e687-29cf-48ce-8bc3-ac8f44f05baa.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 17 of 51 · 1,004 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Fungicure Anti-Fungal Liquid TOLNAFTATE Kobayashi Healthcare International, Inc. b18ee199-0659-733c-e053-2a95a90ab6b5 2026-04-01 Warnings Exact identifier application number: M005 Tolnaftate ANTIFUNGAL LIQUID SPRAY CVS Pharmacy 96cc594d-85c8-4f62-bc0a-3176c8739f21 2026-04-01 Warnings Exact identifier application number: M005 Tolnafate TOLNAFTATE POWDER SPRAY CVS Pharmacy a7b6bd7c-23db-43e1-92f7-e27f5f4801de 2026-04-01 Warnings Exact identifier application number: M005 Baza Antifungal MICONAZOLE NITRATE Coloplast Corp 75182cb7-840a-423a-9c20-10840d6e1d65 2026-03-31 Warnings Exact identifier application number: M005 MICONAZOLE Nitrate 2% Cream ANTIFUNGAL MICONAZOLE NITRATE Trifecta Pharmaceuticals Usa Llc 80217dbb-a0f0-414a-8d22-a9a346b017aa 2026-03-31 Warnings Exact identifier application number: M005 RoyceDerm Antifungal Bar CLOTRIMAZOLE RoyceDerm LLC 3abdc4a8-58dd-5bd0-e063-6294a90a1bca 2026-03-31 Warnings Exact identifier application number: M005 Critic Aid Clear AF MICONAZOLE NITRATE Coloplast Corp cbc5d976-850a-476e-b179-b7a5a8675524 2026-03-31 Warnings Exact identifier application number: M005 Velloryn ANTIFUNGAL Cream ZINC UNDECYLENATE, UNDECYLENIC ACID Guangdong Quadrant Ecological Technology Co., Ltd. 4e38e1f1-0466-5b91-e063-6294a90a66c4 2026-03-30 Warnings Exact identifier application number: M005 APUREE Nailtific Extra-Max Strength Daytime Antigungal APUREE NAILTIFIC EXTRA-MAX STRENGTH DAYTIME ANTIGUNGAL Guangzhou Meixi Biotechnology Co., Ltd. 4e3d226b-57f1-75a6-e063-6394a90a96cd 2026-03-30 Warnings Exact identifier application number: M005 APUREE Nailtific Extra-Max Strength Nighttime Antifungal APUREE NAILTIFIC EXTRA-MAX STRENGTH NIGHTTIME ANTIFUNGAL Guangzhou Meixi Biotechnology Co., Ltd. 4e3e8895-34b4-de69-e063-6294a90a5532 2026-03-30 Exact identifier application number: M005 Miconazole Nitrate ATHLETES FOOT POWDER SPRAY TALC FREE CVS Pharmacy 3380263d-ee7b-4946-a467-35a24789a901 2026-03-27 Warnings Exact identifier application number: M005 Micro-Guard (AF) MICONAZOLE NITRATE Coloplast Corp a43a94d0-fec0-470f-bdb4-535dcce6d1e0 2026-03-27 Warnings Exact identifier application number: M005 Suave Antibacterial Hand Wash Fresh Citrus LIQUID HAND WASH ANTIBACTERIAL Suave Brands Co, LLC 41d77ec6-a1d1-13dc-e063-6394a90a95f4 2026-03-26 Warnings Exact identifier application number: M005 Suave Antibacterial Hand Wash Deeply Clean LIQUID HAND WASH ANTIBACTERIAL Suave Brands Co, LLC 41d83736-66da-abb9-e063-6294a90a3d67 2026-03-26 Warnings Exact identifier application number: M005 Suave Antibacterial Hand Wash Sea Minerals and Aloe Vera LIQUID HAND WASH ANTIBACTERIAL Suave Brands Co, LLC 41d8848c-d157-6e2c-e063-6294a90aa259 2026-03-26 Warnings Exact identifier application number: M005 Hermon Jock Itch Antifungal Treatment Kit Antifungal Cream and .Soap. for Jock Itch ANTIFUNGAL TREATMENT KIT Beautivity LLC 4800a93b-7042-827b-e063-6294a90acd95 2026-03-25 Warnings Exact identifier application number: M005 Toenail Fungus Treatment TERBINAFINE Shenzhen Wankelai E-commerce Co., Ltd. 4dc1d7f7-e4ae-c54b-e063-6394a90aa420 2026-03-24 Warnings Exact identifier application number: M005 Lasolex Liquid Solution CLOTRIMAZOLE 1% PureTek Corporation 4dc9e64d-8235-b218-e063-6394a90a0157 2026-03-24 Warnings Exact identifier application number: M005 Hermon Jock Itch Antifungal Treatment .Soap. Bar TOLNAFTATE 1% Beautivity LLC 4dbbf09b-5bc1-501b-e063-6394a90a2a9d 2026-03-23 Warnings Exact identifier application number: M005 Hermon Jock Itch Antifungal Treatment Cream MICONAZOLE NITRATE 2% Beautivity LLC 4dbc521c-2f5f-9736-e063-6294a90ad85d 2026-03-23 Warnings Exact identifier application number: M005
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76348-401-01 76348040101 11.5 mL in 1 BOTTLE (76348-401-01) 11.5 ml 2011-07-01 No No Current 76348-401-02 76348040102 11.5 mL in 1 BOX (76348-401-02) 11.5 ml 2011-07-01 No No Current