ambrosia artemisiaefolia

Generic: ambrosia artemisiifolia

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

Drug Facts

Product Profile

Brand Name ambrosia artemisiaefolia
Generic Name ambrosia artemisiifolia
Labeler boiron
Dosage Form PELLET
Routes
ORAL
Active Ingredients

ambrosia artemisiifolia 6 [hp_C]/6[hp_C]

Manufacturer
Boiron

Identifiers & Regulatory

Product NDC 0220-0218
Product ID 0220-0218_10e1b09c-a346-f74f-e063-6394a90a3b7c
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 02200218
Hyphenated Format 0220-0218

Supplemental Identifiers

UNII
9W34L2CQ9A

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 ambrosia artemisiaefolia (source: ndc)
Generic Name ambrosia artemisiifolia (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_C]/6[hp_C]
source: ndc
Packaging
  • 6 [hp_C] in 1 TUBE (0220-0218-41)
source: ndc

Packages (1)

0220-0218-41 6 [hp_C] in 1 TUBE (0220-0218-41)

Ingredients (1)

ambrosia artemisiifolia (6 [hp_C]/6[hp_C])

Linked Drug Pages (1)

Ambrosia artemisiaefolia ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10e1b09c-a346-f74f-e063-6394a90a3b7c", "openfda": {"unii": ["9W34L2CQ9A"], "spl_set_id": ["8427439b-f497-5dd7-e053-2991aa0a591b"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0218-41)", "package_ndc": "0220-0218-41", "marketing_start_date": "19830303"}], "brand_name": "Ambrosia artemisiaefolia", "product_id": "0220-0218_10e1b09c-a346-f74f-e063-6394a90a3b7c", "dosage_form": "PELLET", "product_ndc": "0220-0218", "generic_name": "AMBROSIA ARTEMISIIFOLIA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ambrosia artemisiaefolia", "active_ingredients": [{"name": "AMBROSIA ARTEMISIIFOLIA", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}