FREEZE IT Menthol Roll On

SPL

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

Identification

ManufacturerLiquidCapsule Manufacturing LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7172600501
89 mL in 1 BOTTLE, WITH APPLICATOR (71726-005-01)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "33094afe-db9d-4b92-8047-6dd611484fc9": {
      "match": "brand_token",
      "title": "FREEZE IT MENTHOL ROLL ON (MENTHOL) GEL [LIQUIDCAPSULE MANUFACTURING LLC]",
      "spl_version": "1",
      "published_date": "2025-06-09"
    }
  },
  "productid": "71726-005_1fea7e75-1b32-4879-8f9c-47f5503eecb7",
  "productndc": "71726-005",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "FREEZE IT Menthol Roll On",
  "active_ingred_unit": "g/100mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20250605",
  "active_numerator_strength": "3.5"
}

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