FDA.reportPublic FDA data

Hongo Killer

Manufacturer
Efficient Laboratories Inc
Effective date
2011-04-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:51:38

Label at a glance#

ProductHongo Killer
Active ingredientUNDECYLENIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:             Purpose

Undelcylenic Acid 11% v/v ........................ Antifungal


OTC - PURPOSE SECTION


Uses

           For effective treatment of athlete's foot (tinea pedis)
           For the relief of itching, burning feet.
           Clinically proven to prevent Athlete's Foot with daily use.

WARNINGS SECTION


Warnings

For external use only

Flammable: Keep away from fire and flame.

OTC - DO NOT USE SECTION

Do not use on children under 2 years of age, on diaper rash. This product is not effective on the scalp or nails.

When using this product avoid contact with the eyes and mucous membrane.

Stop use and ask doctor if irritation occurs, or there's no improvement within 4 weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast feeding consult a health care professional before using this product.

DOSAGE & ADMINISTRATION SECTION

Directions

  • clean the affected area with soap and water, dry thoroughly
  • Spray a thin layer of Hongo Killer over the affected area twice daily (morning and night) or as directed by a doctor
  • 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.
  • Supervise children in the use of Hongo Killer

INDICATIONS & USAGE SECTION

Other information  store at room temperature 15°- 30°C (59° - 86°F). Do accept if safety seal is broken or missing. Also Hongo Killer is available in Solution, Cream, Powder, Spray Powder and Nail Formula.

Keep box for directions

OTC - QUESTIONS SECTION

Questions or comments?

Please Call 305-805-3456 (M-F 9:00-5:00 pm EST)

www.efficientlabs.com

INACTIVE INGREDIENT SECTION

Inactive ingredients Alcohol Isopropyl, Propionic Acid, Purified Water, Salicylic Acid and Sodium Propionate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HongoKillerSprayLiqHongoKillerSprayLiq

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58593-600-152020-02-19C16284748780-1960f7f55-ca01-8e05-e053-dbdaa90a074aDrug Facts
58593-600-152019-10-29C16284748780-1960f7f55-ca01-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
UNDECYLENIC ACIDACTIVE INGREDIENTK3D86KJ24N3
UNDECYLENIC ACIDACTIVE MOIETYK3D86KJ24N3
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M4163023
PROPIONIC ACIDINACTIVE INGREDIENTJHU490RVYR3
SALICYLIC ACIDINACTIVE INGREDIENTO414PZ4LPZ3
SODIUM PROPIONATEINACTIVE INGREDIENTDK6Y9P42IN3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
58593-60058593-600-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
UNDECYLENIC ACIDK3D86KJ24NACTIB
ISOPROPYL ALCOHOLND2M416302IACT
PROPIONIC ACIDJHU490RVYRIACT
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZIACT
SODIUM PROPIONATEDK6Y9P42INIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 17 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
PROPIONIC ACIDPROPIONIC ACIDJHU490RVYROINTMENT / TOPICAL2.7 %w/wExact identifier — unii candidate
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INCAPSULE / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INSOLUTION / ORAL80 mgExact identifier — unii candidate
7 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INSYRUP / ORAL40 mgExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INPOWDER, FOR SUSPENSION / ORAL12.5 mg/5mlExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INSUSPENSION / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
ISOPROPYL ALCOHOLISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INPOWDER, FOR SOLUTION / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
SODIUM PROPIONATESODIUM PROPIONATEDK6Y9P42INCAPSULE, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates

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
987f5b6f-5b1a-4ffe-8316-f2e84c2bb9821f5ca4ad-fa3f-4852-8011-ad408378c0052011-04-14WarningsExact identifier
spl id: 987f5b6f-5b1a-4ffe-8316-f2e84c2bb982
spl set id: 1f5ca4ad-fa3f-4852-8011-ad408378c005

Reported adverse events (FAERS/openFDA)#

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