Drugplain

UVA URSI 6 [hp_C]/6[hp_C]

ARCTOSTAPHYLOS UVA-URSI LEAF · PELLET · Boiron

No Recall History
Plain English

UVA URSI is a pellet containing arctostaphylos uva-ursi leaf at 6 [hp_C]/6[hp_C], taken oral. Manufactured by Boiron.

Key Facts

Brand Name
UVA URSI
Generic Name
ARCTOSTAPHYLOS UVA-URSI LEAF
NDC Code (Product)
0220-5161
Manufacturer
Boiron
Strength
6 [hp_C]/6[hp_C]
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
03/03/1983

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Directions: FOR ORAL USE ONLY.

Dosage & Administration

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Frequently Asked Questions

What is UVA URSI used for?

UVA URSI contains ARCTOSTAPHYLOS UVA-URSI LEAF. It is a pellet taken oral. Consult your doctor for specific uses.

Is UVA URSI a controlled substance?

UVA URSI is not classified as a controlled substance by the DEA.

What is the generic name for UVA URSI?

The generic name for UVA URSI is ARCTOSTAPHYLOS UVA-URSI LEAF. There are no other listed brand versions of ARCTOSTAPHYLOS UVA-URSI LEAF.

What is the NDC code for UVA URSI 6 [hp_C]/6[hp_C]?

The NDC (National Drug Code) for UVA URSI 6 [hp_C]/6[hp_C] is 0220-5161, listed by Boiron.

Product NDC

0220-5161

Package NDC

0220-5161-41

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)