AsperFlex Original Maximum Strength

SPL

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

Identification

ManufacturerAkron Pharma Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7139944615
5 PATCH in 1 CARTON (71399-4461-5) / 1 PATCH in 1 PATCH

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "117de175-976d-44f3-85ed-3d127fbe3a7c": {
      "match": "brand_token",
      "title": "ASPERFLEX (MENTHOL AND METHYL SALICYLATE) CREAM [AKRON PHARMA INC.]",
      "spl_version": "3",
      "published_date": "2026-01-21"
    }
  },
  "productid": "71399-4461_40333bee-748e-0b43-e063-6394a90a149c",
  "productndc": "71399-4461",
  "dosage_form": "PATCH",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "AsperFlex Original Maximum Strength",
  "active_ingred_unit": "mg/1",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20211104",
  "active_numerator_strength": "210"
}

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