NDC 15631-0702

UVA URSI

Uva Ursi

UVA URSI is a Oral Tablet 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 ID15631-0702_c1347650-44d6-40ff-87ce-63a326326c6b
NDC15631-0702
Product TypeHuman Otc Drug
Proprietary NameUVA URSI
Generic NameUva Ursi
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0702-0

1 TABLET in 1 BLISTER PACK (15631-0702-0)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0702-3 [15631070203]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-6 [15631070206]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-0 [15631070200]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-7 [15631070207]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-1 [15631070201]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-4 [15631070204]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-2 [15631070202]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0702-5 [15631070205]

UVA URSI TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARCTOSTAPHYLOS UVA-URSI LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:fa019cc9-8303-4438-85cb-fb7cbd0c2da8
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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