NDC 71919-700

UVA-URSI

Arctostaphylos Uva-ursi

UVA-URSI is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Arctostaphylos Uva-ursi Leaf.

Product ID71919-700_99c5b0e4-b8cc-c753-e053-2a95a90a6543
NDC71919-700
Product TypeHuman Otc Drug
Proprietary NameUVA-URSI
Generic NameArctostaphylos Uva-ursi
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-05-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameARCTOSTAPHYLOS UVA-URSI LEAF
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-700-07

15 mL in 1 VIAL, GLASS (71919-700-07)
Marketing Start Date2011-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-700-08 [71919070008]

UVA-URSI LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-700-09 [71919070009]

UVA-URSI LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-700-07 [71919070007]

UVA-URSI LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-700-10 [71919070010]

UVA-URSI LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

Drug Details

Active Ingredients

IngredientStrength
ARCTOSTAPHYLOS UVA-URSI LEAF30 [hp_C]/mL

NDC Crossover Matching brand name "UVA-URSI" or generic name "Arctostaphylos Uva-ursi"

NDCBrand NameGeneric Name
68428-691Uva-ursiARCTOSTAPHYLOS UVA-URSI LEAF
71919-700UVA-URSIArctostaphylos uva-ursi

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.