NDC 15631-0452

UVA URSI

Uva Ursi

UVA URSI is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Arctostaphylos Uva-ursi Leaf.

Product ID15631-0452_a1d2e350-aae4-5253-e053-2a95a90a825b
NDC15631-0452
Product TypeHuman Otc Drug
Proprietary NameUVA URSI
Generic NameUva Ursi
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameARCTOSTAPHYLOS UVA-URSI LEAF
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0452-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0452-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0452-5 [15631045205]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0452-0 [15631045200]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0452-3 [15631045203]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0452-2 [15631045202]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0452-1 [15631045201]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0452-4 [15631045204]

UVA URSI PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
ARCTOSTAPHYLOS UVA-URSI LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:0e8cc918-04c6-4051-88a4-4f8e122725db
Manufacturer
UNII

NDC Crossover Matching brand name "UVA URSI" or generic name "Uva Ursi"

NDCBrand NameGeneric Name
0220-5160Uva ursiARCTOSTAPHYLOS UVA URSI LEAF
0220-5161UVA URSIARCTOSTAPHYLOS UVA-URSI LEAF
0220-5162UVA URSIARCTOSTAPHYLOS UVA-URSI LEAF
15631-0452UVA URSIUVA URSI
15631-0702UVA URSIUVA URSI

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