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United States · US · US:58559-001_48617c36-0ba4-cc34-e063-6394a90a0f20

Relief Pain Relieving Cream

SPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerCorganics, LP
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    5855900101
    5 g in 1 BLISTER PACK (58559-001-01)
  • ndc11
    5855900102
    82 g in 1 BOTTLE, WITH APPLICATOR (58559-001-02)
  • ndc11
    5855900103
    115 g in 1 TUBE (58559-001-03)
  • ndc11
    5855900104
    450 g in 1 BOTTLE, PUMP (58559-001-04)
  • ndc11
    5855900105
    3600 g in 1 BOTTLE, PUMP (58559-001-05)

Annotations

DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "route": "TOPICAL",
  "spl_meta": {
    "49e6f0ef-78fb-26fe-e063-6294a90a6655": {
      "match": "brand_token",
      "title": "RELIEF FLEX (MENTHOL) PATCH [BEONE CO., LTD.]",
      "spl_version": "1",
      "published_date": "2026-02-04"
    }
  },
  "productid": "58559-001_48617c36-0ba4-cc34-e063-6394a90a0f20",
  "productndc": "58559-001",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "Relief Pain Relieving Cream",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20040522",
  "active_numerator_strength": "2.5"
}

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