DynaRub

SPL

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

Identification

ManufacturerDynarex Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6777711350
72 TUBE in 1 CASE (67777-113-50) / 85 g in 1 TUBE (67777-113-49)

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "7f853941-a2d7-ed26-e053-2991aa0aa9ee": {
      "match": "brand_token",
      "title": "DYNARUB (PAIN RELIEVING CREAM) CREAM [DYNAREX CORPORATION]",
      "spl_version": "3",
      "published_date": "2024-11-22"
    }
  },
  "productid": "67777-113_275e9d16-0717-f77a-e063-6394a90abb49",
  "productndc": "67777-113",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL; METHYL SALICYLATE",
  "proprietary_name": "DynaRub",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Pain Relieving Cream",
  "start_marketing_date": "20160912",
  "active_numerator_strength": "10; 15"
}

Access this data programmatically

Query DynaRub 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