11673-821 : Up and Up Daytime Vapor Ice Cold and Flu Nighttime Vapor Ice Cold and FluUp and Up Daytime Vapor Ice Cold and Flu Nighttime Vapor Ice Cold and Flu Kit


NDC11673-821
Labeler: Target Corporation
Product Type: Human OTC Drug
Drug Name: Up and Up Daytime Vapor Ice Cold and Flu Nighttime Vapor Ice Cold and Flu
Dosage Form: Kit
Application #: part341
Rev. Date: 


Appearance:


Markings: L35C
L72V
Shapes:  Oval
Colors:  Green
Orange
Size (mm): 19
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 11673-821-90: 1 KIT IN 1 CARTON (11673‑821‑90) * 2 TABLET, FILM COATED IN 1 BLISTER PACK * 2 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Acetaminophen
  • Dextromethorphan Hydrobromide
  • Doxylamine Succinate
  • Phenylephrine Hydrochloride

Kit Contents:

  • Up and Up Daytime Vapor Ice Cold and Flu
  • Up and Up Nighttime Vapor Ice Cold and Flu

Inactive Ingredients:

  • Croscarmellose Sodium
  • Crospovidone (15 Mpa.s At 5%)
  • Fd&c Yellow No. 6
  • Maltodextrin
  • Cellulose, Microcrystalline
  • Polyethylene Glycol
  • Polyvinyl Alcohol
  • Povidone
  • Propylene Glycol
  • Silicon Dioxide
  • Stearic Acid
  • Sucralose
  • Talc
  • Titanium Dioxide /
  • Crospovidone (15 Mpa.s At 5%)
  • D&c Yellow No. 10
  • Fd&c Blue No. 1
  • Fd&c Blue No. 2
  • Fd&c Yellow No. 6
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycol
  • Polyvinyl Alcohol
  • Povidone
  • Propylene Glycol
  • Silicon Dioxide
  • Stearic Acid
  • Sucralose
  • Talc
  • Titanium Dioxide /

Related Products:

Based on records with the same trade name.
  • 11673-477 Up and Up Daytime Vapor Ice Cold and Flu Nighttime Vapor Ice Cold and FluUp and Up Daytime Vapor Ice Cold and Flu Nighttime Vapor Ice Cold and Flu Kit by Target Corporation

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 11673-821 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.