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Hongo Cura RS

Dosage form: cream
Ingredients: ZINC UNDECYLENATE 20g in 100g, UNDECYLENIC ACID 5g in 100g
Labeler: Kramer Laboratories
NDC Code: 55505-146

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.

Zinc undecylenate  20%

Undecylenic acid    5%

antifungal

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

for the treatment of most athletes foot, jock itch and ring worm. for the relief of itchy, scaly skin between the toes. clears most athletes foot infection and with daily use, helps keep it from coming back.

Directions:
• clean the affected area and dry thoroughly
• apply a thin layer of the product 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 the toes, wear well fitting, ventilated shoes, and change shoes and socks at least once daily
• For athletes foot and ring worm, use daily  for 4 weeks.
• for jock itch,  use daily for 2 weeks. If condition persists longer, consult a doctor.


Methylparaben, Propylparaben, white petrolatum

Warnings: For external use only.
Avoid contact with the eyes.
Do not use:
 on children under 2 years of age
 for diaper rash
 on scalp or nails

HONGO CURA  RS
zinc undecylenate undecylenic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55505-146
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC UNDECYLENATE (UNDECYLENIC ACID) ZINC UNDECYLENATE20 g  in 100 g
UNDECYLENIC ACID (UNDECYLENIC ACID) UNDECYLENIC ACID5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
METHYLPARABEN 
PROPYLPARABEN 
PETROLATUM 
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:55505-146-4828 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C12/14/2010
Labeler - Kramer Laboratories (122720675)
Establishment
NameAddressID/FEIOperations
Denison Pharmecuticals001207208manufacture(55505-146)

Revised: 09/2013
 
Kramer Laboratories

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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