Label: HONGO KILLER- undecylenic acid liquid
- NDC Code(s): 58593-826-01
- Packager: Efficient Laboratories Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 2, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
-
DOSAGE & ADMINISTRATION
Directions
Clean the affected area and dry thoroughly.
- Apply
a thin layer of Hongo Killer Antifungal Solution over affected area
twice daily (morning and night) or as directed by a doctor.
- Supervise children in the use of this product.
- For
athlete’s foot: Pay special attention to spaces between 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. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails.
- Apply
a thin layer of Hongo Killer Antifungal Solution over affected area
twice daily (morning and night) or as directed by a doctor.
- INDICATIONS & USAGE
- QUESTIONS
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HONGO KILLER
undecylenic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58593-826 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UNDECYLENIC ACID (UNII: K3D86KJ24N) (UNDECYLENIC ACID - UNII:K3D86KJ24N) UNDECYLENIC ACID 25 mg in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K) ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58593-826-01 30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 07/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 07/01/2012 Labeler - Efficient Laboratories Inc (969044932) Establishment Name Address ID/FEI Business Operations Dextrum Laboratories Inc. 007392322 manufacture(58593-826)