Hongocura ointment

Manufacturer
MENPER DISTRIBUTORS, INC. | RNV, LLC
Effective date
2025-07-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:08:22

Label at a glance#

ProductHongocura
Active ingredientUNDECYLENIC ACID, ZINC UNDECYLENATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients      Purpose

Undecylenic Acid 5%...................Antifungal

Zinc Undecylenate 20%...............Antifungal

OTC - PURPOSE SECTION

Purpose Antifungal

INDICATIONS & USAGE SECTION

Uses:

Proven effective in the treatment of athlete's foot (tinea pedis),jock itch (tinea cruris) and ringworm (tinea corporis).
For the effective relief of itching, burning, crackling and scaly skin between toes.

Clears up athlete's foot infection and with daily use, helps keep it from coming back.

WARNINGS SECTION

Warning:for external use only- Avoid contact with the eyes

Do not use:

On children under 2 years of age, unless directed by a doctor. For diaper rash. This product is not effective on the scalp or nails.

Stop use and ask a doctor if:For athlete's foot and ringworm, if irritation occurs or if there is no improvement within 4 weeks. For jock itch, if irritation occurs or if there is no improvment within 2 weeks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away of reach of children. In case of accidental ingestion, get medical help or contact a Posion Control Center, right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions:

Clean the affected area and dry throughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in use of this product. For athlete's foot: Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks, if condition persists longer, consult a doctor. This product is not effective for the scalp or nails.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Methylparaben, propylparaben and white petrolatum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hongocura OintmentHongocura Ointment

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313552undecylenic acid 5 % / zinc undecylenate 20 % Topical OintmentPSN3
313552undecylenic acid 0.05 MG/MG / zinc undecylenate 0.2 MG/MG Topical OintmentSCD3
313552undecylenic acid 5 % / zinc undecylenate 20 % Topical OintmentSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53145-017-282023-07-28C16284748780-10191ceaa-60fd-198a-e063-dbdaa90aec3eHongocura ointment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53145-017-28Hongocura28 g in 1 TUBEOINTMENT283
53145-017-28Hongocura1 in 1 CARTONOINTMENT13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53145-01753145-017-28

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HongocuraUNDECYLENIC ACID, ZINC UNDECYLENATEMENPER DISTRIBUTORS, INC.c69b735e-0ffe-4328-bd9f-3c1ac6798c082025-07-22WarningsExact identifier
ndc (package): 53145-017-28
ndc (product): 53145-017
ndc11 (package): 53145001728
spl id: 3a8931c9-1449-06ea-e063-6294a90a1df4
spl set id: c69b735e-0ffe-4328-bd9f-3c1ac6798c08

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.