BENZEDREX

UNIISPL

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

Identification

ManufacturerBF ASCHER AND CO INC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0225061123
1 INHALANT in 1 INHALER (0225-0611-23)

Annotations

UNII (FDA Substance ID)

LQU92IU8LL

PROPYLHEXEDRINE

RxCUI 8792

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "LQU92IU8LL",
    "rxcui": "8792",
    "inchikey": "JCRIVQIOJSSCQD-UHFFFAOYSA-N",
    "display_name": "PROPYLHEXEDRINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "NASAL",
  "spl_meta": {
    "00d8c237-3eee-1d9f-e063-6394a90aeb86": {
      "match": "brand_token",
      "title": "BENZEDREX (PROPYLHEXEDRINE) INHALANT [BF ASCHER AND CO INC]",
      "spl_version": "2",
      "published_date": "2024-12-09"
    }
  },
  "productid": "0225-0611_2888acff-4fa4-a9d7-e063-6394a90a7eda",
  "productndc": "0225-0611",
  "dosage_form": "INHALANT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PROPYLHEXEDRINE",
  "proprietary_name": "BENZEDREX",
  "active_ingred_unit": "mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "PROPYLHEXEDRINE",
  "start_marketing_date": "20230623",
  "active_numerator_strength": "175"
}

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