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United States · US · US:71205-314_9608b190-4f25-48f2-a49c-11c360656608

MEDI-FIRST Non-Aspirin Extra Strength

UNIISPLATC N02BE51

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

Identification

ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeN02BE51
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    7120531404
    4 TABLET, FILM COATED in 1 PACKET (71205-314-04)
  • ndc11
    7120531408
    8 TABLET, FILM COATED in 1 PACKET (71205-314-08)

Annotations

UNII (FDA Substance ID)
362O9ITL9D
ACETAMINOPHEN
RxCUI 161
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "362O9ITL9D",
    "rxcui": "161",
    "inchikey": "RZVAJINKPMORJF-UHFFFAOYSA-N",
    "display_name": "ACETAMINOPHEN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "49f04e5d-746d-cbe9-e063-6294a90a7e88": {
      "match": "brand_token",
      "title": "MEDI-FIRST HYDROCORTISONE 1 % ANTI-ITCH CREAM (HYDROCORTISONE) CREAM [UNIFIRST FIRST AID CORPORATION]",
      "spl_version": "4",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71205-314_9608b190-4f25-48f2-a49c-11c360656608",
  "productndc": "71205-314",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ACETAMINOPHEN",
  "proprietary_name": "MEDI-FIRST Non-Aspirin Extra Strength",
  "active_ingred_unit": "mg/1",
  "application_number": "M013",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Acetaminophen",
  "start_marketing_date": "20081230",
  "active_numerator_strength": "500"
}

Related drugs

Other records sharing ATC code N02BE51.

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