NDC 0220-5160

Uva ursi

Arctostaphylos Uva Ursi Leaf

Uva ursi is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Arctostaphylos Uva-ursi Leaf.

• Product ID: 0220-5160_68591b22-b690-6c34-e053-2991aa0ab01f
• NDC: 0220-5160
• Product Type: Human Otc Drug
• Proprietary Name: Uva ursi
• Generic Name: Arctostaphylos Uva Ursi Leaf
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: ARCTOSTAPHYLOS UVA-URSI LEAF
• Active Ingredient Strength: 8 [hp_X]/8[hp_X]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-5160-41

8 [hp_X] in 1 TUBE (0220-5160-41)

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

NDC SPL Data Element Entries

NDC 0220-5160-41 [00220516041]

Uva ursi PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
ARCTOSTAPHYLOS UVA-URSI LEAF	8 [hp_X]/8[hp_X]

OpenFDA Data

• SPL SET ID: 68591b22-b68f-6c34-e053-2991aa0ab01f
• Manufacturer:
  • Boiron
• UNII:
  • 3M5V3D1X36

NDC Crossover Matching brand name "Uva ursi" or generic name "Arctostaphylos Uva Ursi Leaf"

NDC	Brand Name	Generic Name
0220-5160	Uva ursi	ARCTOSTAPHYLOS UVA URSI LEAF
0220-5161	UVA URSI	ARCTOSTAPHYLOS UVA-URSI LEAF
0220-5162	UVA URSI	ARCTOSTAPHYLOS UVA-URSI LEAF
15631-0452	UVA URSI	UVA URSI
15631-0702	UVA URSI	UVA URSI