berberis vulgaris

Generic: berberis vulgaris root bark

Labeler: boiron
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name berberis vulgaris
Generic Name berberis vulgaris root bark
Labeler boiron
Dosage Form PELLET
Routes
ORAL
Active Ingredients

berberis vulgaris root bark 200 [kp_C]/200[kp_C]

Manufacturer
Boiron

Identifiers & Regulatory

Product NDC 0220-0837
Product ID 0220-0837_f2f3a73d-5be6-36c6-e053-2995a90ac478
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1983-03-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02200837
Hyphenated Format 0220-0837

Supplemental Identifiers

UNII
1TH8Q20J0U

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 berberis vulgaris (source: ndc)
Generic Name berberis vulgaris root bark (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 [kp_C]/200[kp_C]
source: ndc
Packaging
  • 200 [kp_C] in 1 TUBE (0220-0837-41)
source: ndc

Packages (1)

0220-0837-41 200 [kp_C] in 1 TUBE (0220-0837-41)

Ingredients (1)

berberis vulgaris root bark (200 [kp_C]/200[kp_C])

Linked Drug Pages (1)

Berberis vulgaris ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f2f3a73d-5be6-36c6-e053-2995a90ac478", "openfda": {"unii": ["1TH8Q20J0U"], "spl_set_id": ["8500b339-58a2-2152-e053-2991aa0a7815"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0837-41)", "package_ndc": "0220-0837-41", "marketing_start_date": "19830303"}], "brand_name": "Berberis vulgaris", "product_id": "0220-0837_f2f3a73d-5be6-36c6-e053-2995a90ac478", "dosage_form": "PELLET", "product_ndc": "0220-0837", "generic_name": "BERBERIS VULGARIS ROOT BARK", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berberis vulgaris", "active_ingredients": [{"name": "BERBERIS VULGARIS ROOT BARK", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}