59672-1716 : Trip Ease Oral Tablet


NDC59672-1716
Labeler: Miers Laboratories
Product Type: Human OTC Drug
Drug Name: Trip Ease
Dosage Form: Oral Tablet
Rev. Date: 


NDC Package Codes:

  • 59672-1716-2: 1 BLISTER PACK IN 1 CARTON (59672‑1716‑2) / 32 TABLET IN 1 BLISTER PACK

Active Ingredients:

  • Anamirta Cocculus Seed
  • Gelsemium Sempervirens Root
  • Sodium Borate
  • Tobacco Leaf
  • Toxicodendron Pubescens Leaf
  • Wood Creosote

Dosage Strength:

  • 30 [hp_C]/1
  • 30 [hp_C]/1
  • 30 [hp_C]/1
  • 30 [hp_C]/1
  • 30 [hp_C]/1
  • 30 [hp_C]/1

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Plant Proteins [CS]

Related Products:

Based on records with the same trade name.
  • 59672-0732 Trip Ease (Sodium Borate 30 [hp_c] / Anamirta Cocculus Seed 30 [hp_c] / Gelsemium Sempervirens Root 30 [hp_c] / Wood Creosote 30 [hp_c] / Toxicodendron Pubescens Leaf 30 [hp_c] / Tobacco Leaf 30 [hp_c]) by Miers Laboratories

NDC QR Code

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NDC 59672-1716 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.