48951-2118 : Berberis Oxalis Oral Liquid


NDC: 48951-2118
Labeler: Uriel Pharmacy Inc.
Product Type: Human OTC Drug
Drug Name: Berberis Oxalis
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 48951-2118-1: 10 AMPULE IN 1 BOX (48951‑2118‑1) > 1 ML IN 1 AMPULE

Active Ingredients:

  • Berberis Vulgaris Root Bark
  • Oxalis Stricta Whole
  • Saw Palmetto
  • Urtica Urens
  • Viscum Album Fruiting Top
  • Magnesium Sulfate
  • Unspecified Form
  • Bos Taurus Prostate Gland
  • Penoxsulam

Dosage Strength:

  • 2 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 4 [hp_X]/mL
  • 6 [hp_X]/mL
  • 8 [hp_X]/mL
  • 10 [hp_X]/mL

Pharmaceutical Classes:

  • Calculi Dissolution Agent [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 48951-2044 Berberis Oxalis Oral Liquid by Uriel Pharmacy Inc.
  • 48951-2045 Berberis Oxalis Oral Pellet by Uriel Pharmacy Inc.
  • 48951-2117 Berberis Oxalis Oral Pellet by Uriel Pharmacy Inc.
  • 48951-2161 Berberis Oxalis Oral Liquid by Uriel Pharmacy Inc.

NDC QR Code

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NDC 48951-2118 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.