lycopodium berberis

Generic: lycopodium berberis

Labeler: uriel pharmacy inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name lycopodium berberis
Generic Name lycopodium berberis
Labeler uriel pharmacy inc.
Dosage Form PELLET
Routes
ORAL
Active Ingredients

berberis vulgaris root bark 3 [hp_X]/1, calomel 10 [hp_X]/1, chelidonium majus root 5 [hp_X]/1, fragaria vesca whole 5 [hp_X]/1, lycopodium clavatum spore 3 [hp_X]/1, milk thistle 1 [hp_X]/1, sulfide ion 6 [hp_X]/1, turmeric 5 [hp_X]/1, vitis vinifera leaf 5 [hp_X]/1

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-6049
Product ID 48951-6049_426390c8-1157-e3af-e063-6394a90a340b
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489516049
Hyphenated Format 48951-6049

Supplemental Identifiers

UNII
1TH8Q20J0U J2D46N657D FLT36UCF0N 5J340B7H82 C88X29Y479 U946SH95EE G15I91XETI 856YO1Z64F R1H893D80E

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lycopodium berberis (source: ndc)
Generic Name lycopodium berberis (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 [hp_X]/1
  • 10 [hp_X]/1
  • 5 [hp_X]/1
  • 1 [hp_X]/1
  • 6 [hp_X]/1
source: ndc
Packaging
  • 1350 PELLET in 1 BOTTLE, GLASS (48951-6049-2)
source: ndc

Packages (1)

48951-6049-2 1350 PELLET in 1 BOTTLE, GLASS (48951-6049-2)

Ingredients (9)

berberis vulgaris root bark (3 [hp_X]/1) calomel (10 [hp_X]/1) chelidonium majus root (5 [hp_X]/1) fragaria vesca whole (5 [hp_X]/1) lycopodium clavatum spore (3 [hp_X]/1) milk thistle (1 [hp_X]/1) sulfide ion (6 [hp_X]/1) turmeric (5 [hp_X]/1) vitis vinifera leaf (5 [hp_X]/1)

Linked Drug Pages (1)

Lycopodium Berberis ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "426390c8-1157-e3af-e063-6394a90a340b", "openfda": {"unii": ["1TH8Q20J0U", "J2D46N657D", "FLT36UCF0N", "5J340B7H82", "C88X29Y479", "U946SH95EE", "G15I91XETI", "856YO1Z64F", "R1H893D80E"], "spl_set_id": ["8312ff6b-4d20-41d4-b736-b50c081c64b6"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1350 PELLET in 1 BOTTLE, GLASS (48951-6049-2)", "package_ndc": "48951-6049-2", "marketing_start_date": "20090901"}], "brand_name": "Lycopodium Berberis", "product_id": "48951-6049_426390c8-1157-e3af-e063-6394a90a340b", "dosage_form": "PELLET", "product_ndc": "48951-6049", "generic_name": "Lycopodium Berberis", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lycopodium Berberis", "active_ingredients": [{"name": "BERBERIS VULGARIS ROOT BARK", "strength": "3 [hp_X]/1"}, {"name": "CALOMEL", "strength": "10 [hp_X]/1"}, {"name": "CHELIDONIUM MAJUS ROOT", "strength": "5 [hp_X]/1"}, {"name": "FRAGARIA VESCA WHOLE", "strength": "5 [hp_X]/1"}, {"name": "LYCOPODIUM CLAVATUM SPORE", "strength": "3 [hp_X]/1"}, {"name": "MILK THISTLE", "strength": "1 [hp_X]/1"}, {"name": "SULFIDE ION", "strength": "6 [hp_X]/1"}, {"name": "TURMERIC", "strength": "5 [hp_X]/1"}, {"name": "VITIS VINIFERA LEAF", "strength": "5 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}