48951-8125 : Renes Betula Oral Liquid


NDC: 48951-8125
Labeler: Uriel Pharmacy Inc.
Product Type: Human OTC Drug
Drug Name: Renes Betula
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 48951-8125-3: 60 ML IN 1 BOTTLE, DROPPER (48951‑8125‑3)

Active Ingredients:

  • Elymus Repens Top
  • Ononis Repens Root
  • Parsley
  • Capsella Bursa-pastoris
  • Arctostaphylos Uva-ursi Leaf
  • Solidago Virgaurea Flowering Top
  • Betula Pubescens Leaf
  • Equisetum Arvense Top
  • Pork Kidney
  • Cytisus Scoparius Flowering Top
  • Copper

Dosage Strength:

  • 2 [hp_X]/mL
  • 2 [hp_X]/mL
  • 2 [hp_X]/mL
  • 2 [hp_X]/mL
  • 2 [hp_X]/mL
  • 2 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 8 [hp_X]/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Copper [CS]
  • Copper-containing Intrauterine Device [EPC]
  • Decreased Embryonic Implantation [PE]
  • Decreased Sperm Motility [PE]
  • Dietary Proteins [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Inhibit Ovum Fertilization [PE]
  • Non-Standardized Food Allergenic Extract [EPC]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Plant Proteins [CS]
  • Vegetable Proteins [CS]

Related Products:

Based on records with the same trade name.
  • 48951-8364 Renes Betula Oral Liquid by Uriel Pharmacy Inc.
  • 48951-8426 Renes Betula Oral Pellet by Uriel Pharmacy Inc.

NDC 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.