ORCA Complete Menthol Pain Reliever

UNIISPL

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

Identification

ManufacturerORCA Products, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8293900002
1 BOTTLE in 1 BOX (82939-000-02) / 13 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)

L7T10EIP3A

MENTHOL, UNSPECIFIED FORM

RxCUI 6750

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "L7T10EIP3A",
    "rxcui": "6750",
    "inchikey": null,
    "display_name": "MENTHOL, UNSPECIFIED FORM",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "99990e27-d66b-4d61-97f2-6a76066eb8b8": {
      "match": "brand_token",
      "title": "ORCA COMPLETE MENTHOL PAIN RELIEVER (MENTHOL) LIQUID [ORCA PRODUCTS, LLC]",
      "spl_version": "3",
      "published_date": "2023-12-11"
    }
  },
  "productid": "82939-000_0c06e3d2-4481-f4b5-e063-6394a90a0608",
  "productndc": "82939-000",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL, UNSPECIFIED FORM",
  "proprietary_name": "ORCA Complete Menthol Pain Reliever",
  "active_ingred_unit": "mg/mL",
  "application_number": "M022",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "MENTHOL",
  "start_marketing_date": "20220915",
  "active_numerator_strength": "20"
}

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