NDC 0295-0100

Benzedrex Nasal Decongestant

Propylhexedrine

Benzedrex Nasal Decongestant is a Nasal Inhalant in the Human Otc Drug category. It is labeled and distributed by Denison Pharmaceuticals Llc. The primary component is Propylhexedrine.

• Product ID: 0295-0100_7ffa790e-a293-8015-e053-2a91aa0a94cb
• NDC: 0295-0100
• Product Type: Human Otc Drug
• Proprietary Name: Benzedrex Nasal Decongestant
• Generic Name: Propylhexedrine
• Dosage Form: Inhalant
• Route of Administration: NASAL
• Marketing Start Date: 2019-01-21
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Denison Pharmaceuticals LLC
• Substance Name: PROPYLHEXEDRINE
• Active Ingredient Strength: 250 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0295-0100-52

1 INHALANT in 1 INHALER (0295-0100-52)

• Marketing Start Date: 2019-01-21
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

Active Ingredients

Ingredient	Strength
PROPYLHEXEDRINE	250 mg/1

OpenFDA Data

• SPL SET ID: 7ffa8df0-803c-b8d4-e053-2991aa0af7ea
• Manufacturer:
  • Denison Pharmaceuticals LLC
• UNII:
  • LQU92IU8LL
• RxNorm Concept Unique ID - RxCUI:
  • 1361538
  • 1361536

NDC Crossover Matching brand name "Benzedrex Nasal Decongestant" or generic name "Propylhexedrine"

NDC	Brand Name	Generic Name
0295-0100	Benzedrex Nasal Decongestant	Propylhexedrine
0225-0610	BENZEDREX	PROPYLHEXEDRINE