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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2096e241-3ed3-49cd-88c4-71db1fd2934a	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
2d2ef081-4f0c-4669-81e8-32b263669a0a	Product name	1	20230801
af534dc0-c9e5-19a6-693c-e7ad53714660	Product name	1	20140508

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
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 42 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tolnaftate	TOLNAFTATE	Sheffield Pharmaceuticals LLC	ca52af37-c3a2-414c-a24a-a37a92925133	2025-02-20	Warnings	Exact identifier application number: M005
Dr Sheffield Athletes Foot	CLOTRIMAZOLE	Sheffield Pharmaceuticals LLC	b8b8e6b2-1022-4592-91ba-3cf94c7cf318	2025-02-19	Warnings	Exact identifier application number: M005
UKVOA Toenail Fungus Treatment	TOLNAFTATE 1% FUNGI NAIL	Jiashen International Trade Limited	2e3cde7b-850e-f9d2-e063-6394a90adb18	2025-02-16	Warnings	Exact identifier application number: M005
UKOVA FOOT ODOR PROBIOTIC	TOLNAFTATE 1% FUNGI NAIL	Jiashen International Trade Limited	2de0225d-dd85-e2da-e063-6294a90a050b	2025-02-11	Warnings	Exact identifier application number: M005
Dr. Scholls Instant Cool Athletes Foot Wipes	TOLNAFTATE	Cosco International, Inc.	cde656a9-7841-4a73-a2f4-f5a76a3e15c1	2025-02-06	Warnings	Exact identifier application number: M005
Silka Athletes Foot	MICONAZOLE NITRATE	Genomma Lab USA	307104a2-2df6-43b0-bf3f-f4d93d3e40f1	2025-02-05	Warnings	Exact identifier application number: M005
MICONAZOLE Nitrate	MICONAZOLE NITRATE	NuCare Pharmaceuticals,Inc.	fd7dd2eb-03a7-ef1f-e053-6294a90a8557	2025-02-04	Warnings	Exact identifier application number: M005
Molecular AF	TOLNAFTATE	Renu Laboratories, LLC	1b47e687-29cf-48ce-8bc3-ac8f44f05baa	2025-02-03	Warnings	Exact identifier application number: M005
Dermatool Fungal Nail Treatment	TOLNAFTATE 1%	Papalo Group LLC	2d2c0e12-123d-75bd-e063-6394a90ae546	2025-01-31	Warnings	Exact identifier application number: M005
70% Isopropyl Alcohol	ISOPROPYL ALCOHOL	IDO PHARM	d5833c6f-81dd-6ff6-e053-2995a90ac76d	2025-01-30	Warnings	Exact identifier application number: M005
AWAS ALCOHOLSPRAY	ALCOHOL	IDO PHARM	03010837-0289-3e08-e063-6394a90a7d04	2025-01-30	Warnings	Exact identifier application number: M005
ELON Dual Defense Anti Fungal Formula	UNDECYLENIC ACID	Little Giant Holdings LLC	45c4567d-7876-6459-e054-00144ff88e88	2025-01-28	Warnings	Exact identifier application number: M005
DCH Labs Antifungal Jock	MICONAZOLE NITRATE 2%	Derma Care Research Labs, LLC	fc749882-2e1e-cad3-e053-6294a90a33ca	2025-01-27	Warnings	Exact identifier application number: M005
Antifungal Pen	UNDECYLENIC ACID 25%	XF Agencija Limited	a15d4512-0fc6-424f-9dd3-ab433d9b7a26	2025-01-27	Warnings	Exact identifier application number: M005
Mata Hongos	UNDECYLENIC ACID	Vitamex USA, Corp	21ca7edb-dde3-5846-e063-6394a90a3cc0	2025-01-23	Warnings	Exact identifier application number: M005
Povidone Iodine Scrub	POVIDONE-IODINE	Jianerkang Medical Co., Ltd	53cb4c0d-40b5-4cf3-b122-fd6dd654883f	2025-01-23	Warnings	Exact identifier application number: M005
NATUREPLEX TOLNAFTATE ANTIFUNGAL	TOLNAFTATE	Natureplex, LLC	575b8645-9166-4242-a74f-f4aa4acaaf3d	2025-01-15	Warnings	Exact identifier application number: M005
Tobcharm Antifungal Treatment Cream	ANTIFUNGAL TREATMENT CREAM	Guangzhou Zanming Trading Co., Ltd.	2ba241cc-2767-1190-e063-6294a90ac66b	2025-01-13	Warnings	Exact identifier application number: M005
MICONAZOLE Nitrate 2%	MICONAZOLE NITRATE	Akron Pharma Inc.	8933f939-098a-4257-8d9c-4d5c3240e9a6	2025-01-10	Warnings	Exact identifier application number: M005
ANTI-ITCH FEMININE CARE	HYDROCORTISONE 0.5%	OL PHARMA TECH, LLC Drs PHARMACY	d6fa5ff3-ebdc-222d-e053-2a95a90a88d5	2025-01-09	Warnings	Exact identifier application number: M005

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
06KB629TKV	TOLNAFTATE	2398-96-1	TOLNAFTATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1236105	hiVETIC 1 % Topical Ointment	PSN	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
199126	tolnaftate 1 % Topical Ointment	PSN	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
1236105	tolnaftate 0.01 MG/MG Topical Ointment [hiVETIC]	SBD	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
199126	tolnaftate 0.01 MG/MG Topical Ointment	SCD	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
1236105	hiVETIC 0.01 MG/MG Topical Ointment	SY	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
1236105	hiVETIC 1 % Topical Ointment	SY	2096e241-3ed3-49cd-88c4-71db1fd2934a	7
199126	tolnaftate 1 % Topical Ointment	SY	2096e241-3ed3-49cd-88c4-71db1fd2934a	7

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