CONAZOL ANTIFUNGAL- tolnaftate solution/ drops 
MarcusUSA

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.

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Conazol®
antifungal

Drug Facts

Active Ingredients

Tolnaftate 1%

Purposes

Antifungal

Uses

For effective treatment of athlete's foot, jock itch and ringworm. Not for relief of infected finger nails and toe nails or effective against bacteria or viruses.

Warnings

For external use only

  • Avoid contact with eyes.
  • Do not use on children under 2 years of age unless directed by a doctor.

Stop and ask a doctor if

  • If treating athlete's foot and ringworm: If irritation occurs or if there is no improvement within 4 weeks.
  • If treating jock itch: If irritation occurs or if there is no improvement within 2 weeks.

Keep out of the reach of children

  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean or wash the affected area and dry thoroughly. Apply a thin layer of the product over the 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 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.

Other Information

Inactive Ingredients

Purified water, PEG-8, Cetearyl alcohol and Ceteth-20 phosphate and decetyl phosphate, Propylene glycol, Cocamidopropyl betaine, Octoxynol-9, Glyceryl stearate, Stearyl alcohol, Hydroxyethyl cellulose, Imidazolidinyl urea, Cetyl alcohol, Methylparaben, Propylparaben, Triethanolamine,Citric acid

Distributed by: MarcasUSA, LLC
El Segundo CA, 90245

PRINCIPAL DISPLAY PANEL - 30 ML Bottle Carton

NOTHING MORE EFFECTIVE

Conazol®
ANTIFUNGAL

TOE FUNGUS
ELIMINATOR

with Tolnaftate 1%

Cures &
Prevents
Fungus

1 FL OZ (30 ML)

Principal Display Panel 30 mL Carton
CONAZOL  ANTIFUNGAL
tolnaftate solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75940-126
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV) Tolnaftate10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)  
propylene glycol (UNII: 6DC9Q167V3)  
cocamidopropyl betaine (UNII: 5OCF3O11KX)  
octoxynol-9 (UNII: 7JPC6Y25QS)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
Stearyl alcohol (UNII: 2KR89I4H1Y)  
HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT)  
IMIDUREA (UNII: M629807ATL)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
methylparaben (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
TROLAMINE (UNII: 9O3K93S3TK)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75940-126-011 in 1 CARTON10/29/2017
130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C10/29/2017
Labeler - MarcusUSA (016139820)
Establishment
NameAddressID/FEIBusiness Operations
Private Label Partners046033481LABEL(75940-126)

Revised: 1/2020
Document Id: 7b6c12bc-8d7c-449e-bef3-c50aeb724142
Set id: 7a6862f1-205c-4880-84dc-7b6776e19713
Version: 2
Effective Time: 20200127
 
MarcusUSA