Benadryl Allergy EXTRA STRENGTH

UNIISPLATC D04AA32

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

Identification

ManufacturerKenvue Brands LLC

CountryUS (United States)

ATC codeD04AA32

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5058053324
2 BLISTER PACK in 1 CARTON (50580-533-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)

TC2D6JAD40

DIPHENHYDRAMINE HYDROCHLORIDE

RxCUI 1362

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "TC2D6JAD40",
    "rxcui": "1362",
    "inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
    "display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8d59d121-62a8-c43b-e053-2a95a90a5847": {
      "match": "brand_token",
      "title": "BENADRYL ALLERGY ULTRATAB (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [SAVINGS DISTRIBUTORS LLC]",
      "spl_version": "3",
      "published_date": "2026-05-13"
    }
  },
  "productid": "50580-533_21731b98-004e-db35-e063-6394a90a8397",
  "productndc": "50580-533",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "proprietary_name": "Benadryl Allergy EXTRA STRENGTH",
  "active_ingred_unit": "mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Diphenhydramine Hydrochloride",
  "start_marketing_date": "20220705",
  "active_numerator_strength": "50"
}

Related drugs

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