58605-315 : Maxi-tuss Pe Max Oral Liquid


NDC58605-315
Labeler: Mcr American Pharmaceuticals, Inc.
Product Type: Human OTC Drug
Drug Name:  Maxi-tuss Pe Max
Dosage Form: Oral Liquid
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 58605-315-16: 473 ML IN 1 BOTTLE, PLASTIC (58605‑315‑16)

Active Ingredients:

  • Guaifenesin
  • Phenylephrine Hydrochloride

Dosage Strength:

  • 100 mg/5mL
  • 5 mg/5mL

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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.