NDC 71919-695

URICUM ACIDUM

Uric Acid

URICUM ACIDUM is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Uric Acid.

Product ID71919-695_99c4f628-9971-ec5c-e053-2a95a90ae5e1
NDC71919-695
Product TypeHuman Otc Drug
Proprietary NameURICUM ACIDUM
Generic NameUric Acid
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-05-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameURIC ACID
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-695-07

15 mL in 1 VIAL, GLASS (71919-695-07)
Marketing Start Date2011-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-695-10 [71919069510]

URICUM ACIDUM LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-695-08 [71919069508]

URICUM ACIDUM LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-695-09 [71919069509]

URICUM ACIDUM LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-695-07 [71919069507]

URICUM ACIDUM LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

Drug Details

Active Ingredients

IngredientStrength
URIC ACID30 [hp_C]/mL

NDC Crossover Matching brand name "URICUM ACIDUM" or generic name "Uric Acid"

NDCBrand NameGeneric Name
71919-695URICUM ACIDUMURIC ACID
63083-1547Uric AcidUric Acid
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.