Home NDC 49873-056 Hi Vetic
Product NDC 49873-056
11-digit product format 498730056
Labeler code 49873
Product ID 49873-056_0bde5831-2b16-2948-e063-6394a90ad473
Type HUMAN OTC DRUG
Nonproprietary name tolnaftate
Dosage form OINTMENT
Route TOPICAL
Labeler Sato Pharmaceutical Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 1996-10-25
Substance TOLNAFTATE
Active strength 1 g/100g
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 Hi Vetic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1 g/100g
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 199126 Internal RxNorm lookup 1236105 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 49873-056-01 Hi Vetic 1 in 1 CARTON OINTMENT 1 7 49873-056-01 Hi Vetic 15 g in 1 TUBE OINTMENT 15 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded tolnaftate ACTIVE INGREDIENT 06KB629TKV HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 tolnaftate ACTIVE MOIETY 06KB629TKV HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 CETETH-20 INACTIVE INGREDIENT I835H2IHHX HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 diethyl sebacate INACTIVE INGREDIENT I41B9FJK6V HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 dimethicone INACTIVE INGREDIENT 92RU3N3Y1O HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 glyceryl monostearate INACTIVE INGREDIENT 230OU9XXE4 HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 light mineral oil INACTIVE INGREDIENT N6K5787QVP HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 POLIDOCANOL INACTIVE INGREDIENT 0AWH8BFG9A HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 potassium stearate INACTIVE INGREDIENT 17V812XK50 HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 propylene glycol INACTIVE INGREDIENT 6DC9Q167V3 HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 silicon INACTIVE INGREDIENT Z4152N8IUI HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 sodium lauryl sulfate INACTIVE INGREDIENT 368GB5141J HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 stearyl alcohol INACTIVE INGREDIENT 2KR89I4H1Y HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 urea INACTIVE INGREDIENT 8W8T17847W HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 water INACTIVE INGREDIENT 059QF0KO0R HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 white wax INACTIVE INGREDIENT 7G1J5DA97F HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4 zinc oxide INACTIVE INGREDIENT SOI2LOH54Z HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49873-056 HI VETIC (TOLNAFTATE) OINTMENT [SATO PHARMACEUTICAL CO., LTD.] 7 Current NDC, Legacy NDC, 2 package rows 20231207_2096e241-3ed3-49cd-88c4-71db1fd2934a.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 48 of 49 · 969 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Signature Black Bottle Tea Tree Antifungal Foot and Body Wash TOLNAFTATE Restoration Rockstar, Llc (dba: Kroning Signature Black Bottle) 2c966d97-30f5-4942-b64d-742884ce6a2f 2023-11-10 Warnings Exact identifier application number: M005 Smooth Gator Fungus Eliminator CLOTRIMAZOLE Smooth Gator, LLC 262b04f5-1b5d-4c67-a557-01f8b1711302 2023-11-10 Warnings Exact identifier application number: M005 TOLNAFTATE ANTIFUNGAL TOLNAFTATE Geri-Care Pharmaceuticals, Corp f9e60430-eec1-4bc2-9522-eb5aa527d90a 2023-11-08 Warnings Exact identifier application number: M005 Terrasil Jock Itch Treatment Maximum Strength CLOTRIMAZOLE Aidance Skincare & Topical Solutions, LLC c62fbf23-5d19-44ab-9c1a-e9b803192ed0 2023-11-08 Warnings Exact identifier application number: M005 terrasil The Fungal Solution Kit CLOTRIMAZOLE Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions 9a5eb581-62a2-41fe-a174-e852fc47e235 2023-11-08 Warnings Exact identifier application number: M005 EmoniNail Antifungal UNDECYLENIC ACID GG Healthworks Inc. 84ace47a-d3ae-4735-87b6-dbbf1c40cf54 2023-11-06 Warnings Exact identifier application number: M005 CIDACIN Antifungal Treatment TOLNAFTATE Pedicis Research LLC bd53a9e3-65c8-4834-8e23-a2a928b83a66 2023-11-05 Warnings Exact identifier application number: M005 MacerRx Web MICONAZOLE NITRATE Clinical Therapeutic Solutions c9327f41-10f1-41f3-855b-838c701d6767 2023-11-05 Warnings Exact identifier application number: M005 CLARUS Antifungal TOLNAFTATE Clinical Therapeutic Solutions 7e8897ff-67d1-4336-866e-cb76a36edddc 2023-11-05 Warnings Exact identifier application number: M005 CLARUS Antifungal TOLNAFTATE Clinical Therapeutic Solutions 308a91d1-3511-4e2d-a62f-a31d77d70e06 2023-11-05 Warnings Exact identifier application number: M005 Human Science Antifungal Foot Care UNDECYLENIC ACID HUMAN SCIENCE, LLC 26b2519b-7d7b-4b33-b5d6-a41fe6f73538 2023-11-05 Warnings Exact identifier application number: M005 HomeHealth Antifungal TOLNAFTATE Home Health 895cd24c-3f78-4e2e-bf98-8bb6605798da 2023-11-05 Warnings Exact identifier application number: M005 Clotrimazole CLOTRIMAZOLE Proficient Rx LP 800a9dab-d287-427e-af6d-26996e0def41 2023-11-01 Warnings Exact identifier application number: M005 Povidone Iodine POVIDONE-IODINE Dr Radows 58e1757c-45ce-455e-bd64-a9e99cd3680f 2023-10-30 Warnings Exact identifier application number: M005 JOCK-EZE CLOTRIMAZOLE Bentlin Products LLC d3ff5bfb-2e0f-4daa-84b3-4a3016ca9280 2023-10-30 Warnings Exact identifier application number: M005 TheraPlus Plus CLOTRIMAZOLE Zhejiang Jingwei Pharmaceutical Co., Ltd. de75179d-1889-4823-9f39-4bebdf185d76 2023-10-27 Warnings Exact identifier application number: M005 Evercare Antifungal Treatment Super Absorbent Powder MICONAZOLE NITRATE PANEFFORT, LLC f91910f3-b461-43a4-9120-fda69483fffa 2023-10-26 Warnings Exact identifier application number: M005 Thera plus Antifungal Clotrimazole CLOTRIMAZOLE FOURSTAR GROUP USA, INC. 1265be99-8922-4b76-bd63-19bfb42c3896 2023-10-26 Warnings Exact identifier application number: M005 Thera plus Antifungal Tolnaftate TOLNAFTATE FOURSTAR GROUP USA, INC. c628dda8-7a6d-5f3a-e053-2995a90a35f8 2023-10-26 Warnings Exact identifier application number: M005 Povidone Iodine POVIDONE IODINE Jianerkang Medical Co., Ltd e1789944-3a41-4c86-b173-3a6993ae2141 2023-10-23 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 Marketing end Sample Exclude flag Status 49873-056-01 49873005601 1 TUBE in 1 CARTON (49873-056-01) / 15 g in 1 TUBE 1 tube 1996-10-25 0000-00-00 No No Current