Urodel Homeopathic Urinary Tract Infection

Product NDC
55758-308
Requested package NDC
55758-308-30
11-digit product format
557580308
Labeler code
55758
Product ID
55758-308_f05e2b3e-be9b-5187-e053-2a95a90a1067
Type
HUMAN OTC DRUG
Nonproprietary name
Cantharis, Clematis, Cubeba, Echinacea, Ranunculus bulbosus, Sabal ser, Staphysagria, Uva ursi
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Pharmadel LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-01-08
Marketing end
0000-00-00
Substance
ARCTOSTAPHYLOS UVA-URSI LEAF; CLEMATIS RECTA FLOWERING TOP; DELPHINIUM STAPHISAGRIA SEED; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA; PIPER CUBEBA FRUIT; RANUNCULUS BULBOSUS; SAW PALMETTO
Active strength
6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage55758-30855758-308-30DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55758-308-30557580308301 BOTTLE in 1 CARTON (55758-308-30) > 30 TABLET, CHEWABLE in 1 BOTTLE1 bottle2022-03-150000-00-00NoNoCurrent