48951-2157 : Berberis Larix Oral Pellet


NDC48951-2157
Labeler: Uriel Pharmacy Inc
Product Type: Human OTC Drug
Drug Name: Berberis Larix
Dosage Form: Oral Pellet
Rev. Date: 


NDC Package Codes:

  • 48951-2157-2: 1350 PELLET IN 1 BOTTLE, GLASS (48951‑2157‑2)

Active Ingredients:

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

Dosage Strength:

  • 3 [hp_X]/1
  • 8 [hp_X]/1
  • 3 [hp_X]/1
  • 3 [hp_X]/1
  • 8 [hp_X]/1
  • 8 [hp_X]/1
  • 6 [hp_X]/1
  • 8 [hp_X]/1

Pharmaceutical Classes:

  • Allergens [CS]
  • Bee Venoms [CS]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Standardized Insect Venom Allergenic Extract [EPC]

Related Products:

Based on records with the same trade name.
  • 48951-2119 Berberis Larix Oral Pellet by Uriel Pharmacy Inc
  • 48951-2042 Berberis Larix Oral Liquid 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.