NDC 0220-5335

Xanthoxylum fraxineum

Zanthoxylum Americanum Bark

Xanthoxylum fraxineum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Zanthoxylum Americanum Bark.

• Product ID: 0220-5335_8143ad9d-702a-fa2f-e053-2a91aa0a33ac
• NDC: 0220-5335
• Product Type: Human Otc Drug
• Proprietary Name: Xanthoxylum fraxineum
• Generic Name: Zanthoxylum Americanum Bark
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: ZANTHOXYLUM AMERICANUM BARK
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-5335-41

30 [hp_C] in 1 TUBE (0220-5335-41)

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

NDC SPL Data Element Entries

NDC 0220-5335-41 [00220533541]

Xanthoxylum fraxineum PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
ZANTHOXYLUM AMERICANUM BARK	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 8143ad9d-7029-fa2f-e053-2a91aa0a33ac
• Manufacturer:
  • Boiron
• UNII:
  • A4KL1HMZ7T

NDC Crossover Matching brand name "Xanthoxylum fraxineum" or generic name "Zanthoxylum Americanum Bark"

NDC	Brand Name	Generic Name
0220-5335	Xanthoxylum fraxineum	ZANTHOXYLUM AMERICANUM BARK
15631-0465	XANTHOXYLUM FRAXINEUM	XANTHOXYLUM FRAXINEUM
68428-709	Xanthoxylum fraxineum	ZANTHOXYLUM AMERICANUM BARK
71919-720	XANTHOXYLUM FRAXINEUM	Zanthoxylum americanum
64117-296	HEADCHES PAINFUL MENSTRUATION	ZANTHOXYLUM AMERICANUM BARK