DB ANTIFUNGAL FOOT- miconazole nitrate cream 
The Magni Group Inc

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DB Antifungal foot

Drug Facts

Active ingredients (in cream)

Miconazole Nitrate 2%

Purpose

Antifungal

Uses

• Cures most tinea pedis (athlete’s foot) • Relieves itching, scaling, cracking, burning, redness; itchy, scaly skin between toes; itching, burning feet; discomfort

Warnings

Do not use

  • on children under 2 years of age unless directed by a doctor • For external use only
  • Avoid contact with the eyes 
  • If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor

Keep out of reach of children

• If swallowed, get medical attention, 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 spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily • For athlete’s foot and ringworm, use daily for 4 weeks; for jock itch, use daily for 2 weeks • If condition persists longer, consult a doctor • This product is not effective on the scalp or nails

Inactive ingredients

Allium Sativum Garlic (Plant) Extract, C12-15 Alkyl Benzoate, Ceteth-20, Cetyl Alcohol, Ethylhexylglycerin, Eucalyptus Globulus Leaf Oil, Garcinia Indica Seed Butter, Hydroxyacetophenone, Isopropyl Palmitate, Isopropyl Myristate, Lemon Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Phenoxyethanol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sodium Acrylate/Sodium Acryldimethyl Taurate Copolymer, Tocopheryl Acetate, Water

Package Labeling:

Label

DB ANTIFUNGAL FOOT 
miconazole nitrate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43689-0025
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
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CETETH-20 (UNII: I835H2IHHX)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GARCINIA INDICA SEED BUTTER (UNII: US2H3D7800)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
LEMON OIL (UNII: I9GRO824LL)  
TEA TREE OIL (UNII: VIF565UC2G)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ALMOND OIL (UNII: 66YXD4DKO9)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43689-0025-1113 g in 1 JAR; Type 0: Not a Combination Product04/27/2017
2NDC:43689-0025-21 in 1 BOX04/27/2017
2113 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00504/27/2017
Labeler - The Magni Group Inc (113501902)

Revised: 10/2023
Document Id: 08854bfe-b2c1-e134-e063-6394a90a773f
Set id: e206738e-6b24-4b03-a84f-7c2521d022ea
Version: 5
Effective Time: 20231025
 
The Magni Group Inc