benzedrex

Generic: propylhexedrine

Labeler: bf ascher and co inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benzedrex
Generic Name propylhexedrine
Labeler bf ascher and co inc
Dosage Form INHALANT
Routes
NASAL
Active Ingredients

propylhexedrine 175 mg/1

Manufacturer
BF ASCHER AND CO INC

Identifiers & Regulatory

Product NDC 0225-0611
Product ID 0225-0611_2888acff-4fa4-a9d7-e063-6394a90a7eda
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-06-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02250611
Hyphenated Format 0225-0611

Supplemental Identifiers

UNII
LQU92IU8LL

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name benzedrex (source: ndc)
Generic Name propylhexedrine (source: ndc)
Application Number M012 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 175 mg/1
source: ndc
Packaging
  • 1 INHALANT in 1 INHALER (0225-0611-23)
source: ndc

Packages (1)

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

Ingredients (1)

propylhexedrine (175 mg/1)

Linked Drug Pages (1)

BENZEDREX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "2888acff-4fa4-a9d7-e063-6394a90a7eda", "openfda": {"unii": ["LQU92IU8LL"], "spl_set_id": ["00d8c237-3eee-1d9f-e063-6394a90aeb86"], "manufacturer_name": ["BF ASCHER AND CO INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALANT in 1 INHALER (0225-0611-23)", "package_ndc": "0225-0611-23", "marketing_start_date": "20230623"}], "brand_name": "BENZEDREX", "product_id": "0225-0611_2888acff-4fa4-a9d7-e063-6394a90a7eda", "dosage_form": "INHALANT", "product_ndc": "0225-0611", "generic_name": "PROPYLHEXEDRINE", "labeler_name": "BF ASCHER AND CO INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BENZEDREX", "active_ingredients": [{"name": "PROPYLHEXEDRINE", "strength": "175 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230623", "listing_expiration_date": "20261231"}