NDC 0067-2083

COMTREX Maximum Strength Day / Night Severe Cold and Sinus

Acetaminophen, Chlorpheniramine Maleate, Phenylephrin Hcl

COMTREX Maximum Strength Day / Night Severe Cold and Sinus is a Kit in the Human Otc Drug category. It is labeled and distributed by Novartis Consumer Health, Inc.. The primary component is .

• Product ID: 0067-2083_801d3659-d0e8-4c3b-ac03-4fc0b9b211dc
• NDC: 0067-2083
• Product Type: Human Otc Drug
• Proprietary Name: COMTREX Maximum Strength Day / Night Severe Cold and Sinus
• Generic Name: Acetaminophen, Chlorpheniramine Maleate, Phenylephrin Hcl
• Dosage Form: Kit
• Marketing Start Date: 2010-07-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Novartis Consumer Health, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 0067-2083-24

3 BLISTER PACK in 1 CARTON (0067-2083-24) > 1 KIT in 1 BLISTER PACK

• Marketing Start Date: 2010-07-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0067-2083-24 [00067208324]

COMTREX Maximum Strength Day / Night Severe Cold and Sinus KIT

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-07-01
• Marketing End Date: 2013-02-12

Drug Details

OpenFDA Data

• SPL SET ID: 801d3659-d0e8-4c3b-ac03-4fc0b9b211dc
• Manufacturer:
  • Novartis Consumer Health, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 1046378
  • 1046781
  • 1244951
• UPC Code:
  • 0300672083241