Benadryl Allergy

UNIISPLATC D04AA32

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

Identification

ManufacturerR J General Corporation

CountryUS (United States)

ATC codeD04AA32

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7026402401
30 POUCH in 1 CARTON (70264-024-01) / 2 TABLET, FILM COATED in 1 POUCH

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": "70264-024_43c8a290-73a2-52bb-e063-6294a90af527",
  "productndc": "70264-024",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "proprietary_name": "Benadryl Allergy",
  "active_ingred_unit": "mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "start_marketing_date": "20220301",
  "active_numerator_strength": "25"
}

Related drugs

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