foot powder

Generic: miconazole nitrate

Labeler: walgreens company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foot powder
Generic Name miconazole nitrate
Labeler walgreens company
Dosage Form POWDER
Routes
TOPICAL
Active Ingredients

miconazole nitrate 20 mg/g

Manufacturer
Walgreens Company

Identifiers & Regulatory

Product NDC 0363-7999
Product ID 0363-7999_49786c9d-1a64-2c80-e063-6394a90a7150
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M005
Listing Expiration 2027-12-31
Marketing Start 2024-03-12

Pharmacologic Class

Classes
azole antifungal [epc] azoles [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03637999
Hyphenated Format 0363-7999

Supplemental Identifiers

RxCUI
998461
UPC
0311917052090
UNII
VW4H1CYW1K

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name foot powder (source: ndc)
Generic Name miconazole nitrate (source: ndc)
Application Number M005 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/g
source: ndc
Packaging
  • 71 g in 1 BOTTLE, PLASTIC (0363-7999-01)
  • 85 g in 1 BOTTLE, PLASTIC (0363-7999-03)
source: ndc

Packages (2)

0363-7999-01 71 g in 1 BOTTLE, PLASTIC (0363-7999-01) 0363-7999-03 85 g in 1 BOTTLE, PLASTIC (0363-7999-03)

Ingredients (1)

miconazole nitrate (20 mg/g)

Linked Drug Pages (1)

Foot Powder ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "49786c9d-1a64-2c80-e063-6394a90a7150", "openfda": {"upc": ["0311917052090"], "unii": ["VW4H1CYW1K"], "rxcui": ["998461"], "spl_set_id": ["137a493b-6ed5-d649-e063-6294a90ac442"], "manufacturer_name": ["Walgreens Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "71 g in 1 BOTTLE, PLASTIC (0363-7999-01)", "package_ndc": "0363-7999-01", "marketing_start_date": "20240312"}, {"sample": false, "description": "85 g in 1 BOTTLE, PLASTIC (0363-7999-03)", "package_ndc": "0363-7999-03", "marketing_start_date": "20251217"}], "brand_name": "Foot Powder", "product_id": "0363-7999_49786c9d-1a64-2c80-e063-6394a90a7150", "dosage_form": "POWDER", "pharm_class": ["Azole Antifungal [EPC]", "Azoles [CS]"], "product_ndc": "0363-7999", "generic_name": "Miconazole Nitrate", "labeler_name": "Walgreens Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foot Powder", "active_ingredients": [{"name": "MICONAZOLE NITRATE", "strength": "20 mg/g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240312", "listing_expiration_date": "20271231"}