Walgreens Medicated Foot Powder

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerDavion, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4266910010
283 g in 1 BOTTLE (42669-100-10)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "34952272-1f9e-c642-e063-6394a90ae2bd": {
      "match": "brand_token",
      "title": "WALGREENS SCALP ITCH RELIEF (HYDROCORTISONE) LIQUID [WALGREENS]",
      "spl_version": "2",
      "published_date": "2026-06-01"
    }
  },
  "productid": "42669-100_f0cf82f2-4010-4eab-9c98-ac57c53dccc7",
  "productndc": "42669-100",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "Walgreens Medicated Foot Powder",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20180601",
  "active_numerator_strength": "1"
}

Access this data programmatically

Query Walgreens Medicated Foot Powder and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs