48951-2042 : Berberis Larix Oral Liquid


NDC48951-2042
Labeler: Uriel Pharmacy Inc.
Product Type: Human OTC Drug
Drug Name: Berberis Larix
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 48951-2042-1: 10 AMPULE IN 1 BOX (48951‑2042‑1) > 1 ML IN 1 AMPULE

Active Ingredients:

  • Achillea Millefolium
  • Berberis Vulgaris Root Bark
  • Equisetum Arvense Top
  • Lytta Vesicatoria
  • Apis Mellifera
  • Ferrous Disulfide
  • Larix Decidua Resin
  • Sus Scrofa Urinary Bladder

Dosage Strength:

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

Related Products:

Based on records with the same trade name.
  • 48951-2119 Berberis Larix Oral Pellet by Uriel Pharmacy Inc
  • 48951-2157 Berberis Larix Oral Pellet by Uriel Pharmacy Inc

NDC QR Code

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NDC 48951-2042 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.