0067-0105 : Theraflu Oral Syrup


NDC: 0067-0105
Labeler: Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
Product Type: Human OTC Drug
Drug Name:  Theraflu Severe Cold Relief Nighttime
Dosage Form: Oral Syrup
Application #: M012
Rev. Date: 


NDC Package Codes:

  • 0067-0105-08: 245.5 ML IN 1 BOTTLE (0067‑0105‑08)

Active Ingredients:

  • Acetaminophen
  • Diphenhydramine Hydrochloride

Dosage Strength:

  • 650 mg/30mL
  • 25 mg/30mL

Pharmaceutical Classes:

  • Histamine H1 Receptor Antagonists [MoA]
  • Histamine-1 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0067-0101 Theraflu Severe Cold Relief Nighttime Oral Powder, for Solution by Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
  • 0067-6800 Theraflu Severe Cold Relief Nighttime Oral Powder by Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
  • 0067-6801 Theraflu Severe Cold Relief Nighttime Oral Powder by Glaxosmithkline Consumer Healthcare Holdings (Us) LLC
  • 0067-6803 Theraflu Oral Powder, for Solution by Haleon Us Holdings LLC
  • 50269-101 Theraflu Severe Cold Relief Nighttime Oral Powder, for Solution by Jc World Bell Wholesale Co., Inc.

NDC QR Code

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NDC 0067-0105 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.