NDC 33992-5561

Pain Relief PM Extra Relief

Acetaminophen 500 Mg, Diphenhydramine Hcl 25 Mg

Pain Relief PM Extra Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Greenbrier International, Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

• Product ID: 33992-5561_3205bcf5-7142-45ca-96a4-96ffdb925418
• NDC: 33992-5561
• Product Type: Human Otc Drug
• Proprietary Name: Pain Relief PM Extra Relief
• Generic Name: Acetaminophen 500 Mg, Diphenhydramine Hcl 25 Mg
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2007-12-17
• Marketing End Date: 2019-07-08
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: GREENBRIER INTERNATIONAL, INC.
• Substance Name: ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
• Active Ingredient Strength: 500 mg/1; mg/1
• NDC Exclude Flag: N

Packaging

NDC 33992-5561-0

1 BOTTLE in 1 CARTON (33992-5561-0) > 40 TABLET in 1 BOTTLE

• Marketing Start Date: 2007-12-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 33992-5561-0 [33992556100]

Pain Relief PM Extra Relief TABLET

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2007-12-17
• Marketing End Date: 2019-07-08

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	500 mg/1

OpenFDA Data

• SPL SET ID: 82b85ef8-25cd-446d-999b-19db33bb7a95
• Manufacturer:
  • GREENBRIER INTERNATIONAL, INC.
• UNII:
  • TC2D6JAD40
  • 362O9ITL9D
• RxNorm Concept Unique ID - RxCUI:
  • 1092189
• UPC Code:
  • 0639277066107