LOTRIMIN AF ANTIFUNGAL- miconazole nitrate spray 
Bayer Healthcare LLC.

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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Lotrimin ® AF

Antifungal Liquid

Drug Facts

Active ingredient

(To Deliver) Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only

Flammable

Do not use while smoking or near heat or flame

Do not use on children under 2 years of age unless directed by a doctor

When using this product

  • avoid contact with the eyes
  • use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal
  • Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask a doctor if

  • irritation occurs
  • there is no improvement within 4 weeks (for athlete's foot and ringworm) or 2 weeks (for jock itch)

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

Directions

Other information

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

dimethyl ether, polyoxyl 15 hydroxystearate, sd alcohol 40-B (16.5% v/v)

Questions?

1-866-360-3266

Distribution

Distributed by Bayer HealthCare LLC

Whippany, NJ 07981 USA

PRINCIPAL DISPLAY PANEL - 133 g Can Label

Liquid Spray

cools the burn

NDC 11523-4327-01

LOTRIMIN®AF

ANTIFUNGAL

miconazole nitrate

Clinically Proven To Cure

Most Athlete's Foot

NET WT 133g (4.6 OZ)

Label 133 g

LOTRIMIN AF  ANTIFUNGAL
miconazole nitrate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4327
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
DIMETHYL ETHER (UNII: AM13FS69BX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-4327-1133 g in 1 CAN; Type 0: Not a Combination Product09/01/1993
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333C09/01/1993
Labeler - Bayer Healthcare LLC. (112117283)

Revised: 9/2023
Document Id: 0554c671-0715-3eb9-e063-6394a90ab956
Set id: d6eb3b78-405b-43e5-9db5-da671465eda1
Version: 8
Effective Time: 20230914
 
Bayer Healthcare LLC.