CONAZOL ANTIFUNGAL- tolnaftate solution/ drops

Conazol by

Drug Labeling and Warnings

Conazol by is a Otc medication manufactured, distributed, or labeled by MarcusUSA, Private Label Partners. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

• Store at room temperature 15°-30°C (59°-86°F)

QUESTIONS

• Questions or comments, call (800) 428-9489

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

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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)

INGREDIENTS AND APPEARANCE

CONAZOL  ANTIFUNGAL
tolnaftate solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75940-126
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV)	Tolnaftate	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75940-126-01	1 in 1 CARTON	10/29/2017
1		30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	10/29/2017

Labeler - MarcusUSA (016139820)

Establishment
Name	Address	ID/FEI	Business Operations
Private Label Partners		046033481	LABEL(75940-126)