SUNMED pain freeze

SPL

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

Identification

ManufacturerSunflora Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7324090401
89 mL in 1 BOTTLE, PLASTIC (73240-904-01)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "ff49699c-ced9-13d2-e053-6394a90af079": {
      "match": "brand_token",
      "title": "SUNMED PAIN FREEZE (MENTHOL) SPRAY [SUNFLORA INC.]",
      "spl_version": "2",
      "published_date": "2025-08-21"
    }
  },
  "productid": "73240-904_3cbd785f-2ab1-56e2-e063-6294a90a65fc",
  "productndc": "73240-904",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "SUNMED pain freeze",
  "active_ingred_unit": "g/100mL",
  "application_number": "M017.10",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20250819",
  "active_numerator_strength": "6"
}

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