0067-6802 : Theraflu Oral Powder, for Solution


NDC: 0067-6802
Labeler: Haleon Us Holdings LLC
Product Type: Human OTC Drug
Drug Name: Theraflu Severe Cold Relief Daytime
Dosage Form: Oral Powder, for Solution
Application #: M012
Rev. Date: 


NDC Package Codes:

  • 0067-6802-02: 6 PACKET IN 1 CARTON (0067‑6802‑02) / 237 ML IN 1 PACKET

Active Ingredients:

  • Acetaminophen
  • Dextromethorphan Hydrobromide
  • Phenylephrine Hydrochloride

Dosage Strength:

  • 500 mg/237mL
  • 20 mg/237mL
  • 10 mg/237mL

Pharmaceutical Classes:

  • Adrenergic alpha1-Agonists [MoA]
  • Sigma-1 Agonist [EPC]
  • Sigma-1 Receptor Agonists [MoA]
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]
  • Uncompetitive NMDA Receptor Antagonists [MoA]
  • alpha-1 Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0067-0100 Theraflu Severe Cold Relief Daytime Oral Powder, for Solution by Glaxosmithkline Consumer Healthcare Holdings (Us) LLC

NDC QR Code

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NDC 0067-6802 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.