MICONAZOLE NITRATE- antifungal liquid continuous spray aerosol, spray 
HEB

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HEB Antifungal Miconazole Liquid Continuous Spray

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Uses

Warnings

For external use only.

Extremely flammable:

Content under pressure. Keep away from fire, sparks and heated surfaces. Do not punchure or incinerate container. Exposure to temperatures above 120 oF may cause bursting. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

Do not use

on children under 2 years of age unless directed by a doctor.

When using this product

  • avoid contact with the eyes or mouth
  • use only as directed

Stop use and ask a doctor if

  • no improvement within 4 weeks for athlete's foot and ringworm and 2 weeks for jock itch
  • irritation occurs

Keep out of reach of children.

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

Directions

Other information

store between 20º and 30ºC (68º and 86ºF)

Inactive ingredients

acetone, ethoxydiglycol, propylene glycol, SD alcohol 40-B (74%w/w), tocopheryl acetate

Questions?

Call 1-866-964-0939

Principal Display Panel

HEB

Antifungal

Miconazole Nitrate 2%

Liquid Continuous Spray

NET WT 5.3 OZ (150g)

H-E-B_Antifungal Miconazole Continuous Liquid Spray_ALMCSHEB-1.jpg

MICONAZOLE NITRATE 
antifungal liquid continuous spray aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-520
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE3 g  in 150 g
Inactive Ingredients
Ingredient NameStrength
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALCOHOL (UNII: 3K9958V90M)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ACETONE (UNII: 1364PS73AF)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-520-53150 g in 1 CAN; Type 0: Not a Combination Product01/17/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00501/17/2012
Labeler - HEB (007924756)

Revised: 1/2024
Document Id: 10309405-c210-a4f2-e063-6394a90a3b68
Set id: bfa0ba85-f88b-4610-8538-2f6e1b444516
Version: 5
Effective Time: 20240130
 
HEB