48951-3134 : Crataegus Nicotiana Oral Liquid


NDC: 48951-3134
Labeler: Uriel Pharmacy Inc.
Product Type: Human OTC Drug
Drug Name: Crataegus Nicotiana
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 48951-3134-1: 10 AMPULE IN 1 BOX (48951‑3134‑1) > 1 ML IN 1 AMPULE

Active Ingredients:

  • Hawthorn Leaf With Flower
  • Cerium
  • Beef Heart
  • Magnesium Phosphate
  • Tribasic
  • Pentahydrate
  • Tobacco Leaf

Dosage Strength:

  • 3 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 10 [hp_X]/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Calculi Dissolution Agent [EPC]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Plant Proteins [CS]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 48951-3135 Crataegus Nicotiana Oral Pellet by Uriel Pharmacy Inc.

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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.