CONAZOL- miconazole nitrate cream

Conazol by

Drug Labeling and Warnings

Conazol by is a Otc medication manufactured, distributed, or labeled by Laboratorios Liomont, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

• effective in the treatment of most athlete's foot, jock itch and ringworm
• relieves itching, cracking, burning and discomfort associated with these conditions

Warnings

For external use only

Do not use

on children less than 2 years of age unless directed by a doctor

When using this product

avoid contact with the eyes

Stop use and ask a doctor if

• irritation occurs
• there is no improvement of athlete's foot or ringworm within 4 weeks or jock itch within 2 weeks

Keep out of reach of children

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

Directions

• wash 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 the spaces between the toes; wear well-fitting, ventilated shoes,and change shoes

and socks at least once daily

• for the athlete's foot and ringworm, use daily for 4 weeks
• for jock itch, use daily for 2 weeks
• not effective on the scalp or nails

Other Information

• store at 20° to 25°C (68° to 77°F)

Inactive Ingredients

butylated hydroxyanisole, caprylic/capic triglyceride,carbomer 980, emulsifying wax, glycerin, methylparaben, propylene glycol, propylparaben, purified water, triethanolamine

Package Label

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INGREDIENTS AND APPEARANCE

CONAZOL 
miconazole nitrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59208-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59208-001-30	30 g in 1 TUBE; Type 0: Not a Combination Product	03/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	03/01/2019

Labeler - Laboratorios Liomont, S.A. de C.V. (810347807)

Establishment
Name	Address	ID/FEI	Business Operations
Laboratorios Liomont, S.A. de C.V.		810347807	manufacture(59208-001)