NDC 0220-5307

Wyethia helenioides

Wyethia Helenioides Root

Wyethia helenioides is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Laboratoires Boiron. The primary component is Wyethia Helenioides Root.

• Product ID: 0220-5307_60145740-0661-e835-e053-2991aa0abde7
• NDC: 0220-5307
• Product Type: Human Otc Drug
• Proprietary Name: Wyethia helenioides
• Generic Name: Wyethia Helenioides Root
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Laboratoires Boiron
• Substance Name: WYETHIA HELENIOIDES ROOT
• Active Ingredient Strength: 6 [hp_C]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-5307-41

80 PELLET in 1 TUBE (0220-5307-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-5307-41 [00220530741]

Wyethia helenioides PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
WYETHIA HELENIOIDES ROOT	6 [hp_C]/1

OpenFDA Data

• SPL SET ID: d7a886f0-7c76-11e6-8aae-424c58303031
• Manufacturer:
  • Laboratoires Boiron
• UNII:
  • J10PD1AQ0N

NDC Crossover Matching brand name "Wyethia helenioides" or generic name "Wyethia Helenioides Root"

NDC	Brand Name	Generic Name
0220-5307	Wyethia helenioides	WYETHIA HELENIOIDES ROOT
0220-5308	WYETHIA HELENIOIDES	WYETHIA HELENIOIDES ROOT
15631-0464	WYETHIA HELENIOIDES	WYETHIA HELENIOIDES
68428-708	Wyethia helenioides	WYETHIA HELENIOIDES ROOT
71919-719	WYETHIA HELENIOIDES	WYETHIA HELENIOIDES
64117-198	Sore Throat Dry Cough	WYETHIA HELENIOIDES ROOT