Home NDC 43689-0057 Bladder Relief
Product NDC 43689-0057
11-digit product format 436890057
Labeler code 43689
Product ID 43689-0057_ce5b0b46-200c-4aad-a550-fb965099721a
Type HUMAN OTC DRUG
Nonproprietary name Causticum, Natrum Muriaticum, Nux Vomica, Pulsatilla (Vulgaris), Sepia, Staphysagria, Thuja Occidentalis
Dosage form TABLET
Route ORAL
Labeler The Magni Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-03-14
Substance CAUSTICUM; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS WHOLE; SEPIA OFFICINALIS JUICE; DELPHINIUM STAPHISAGRIA SEED; THUJA OCCIDENTALIS LEAFY TWIG
Active strength 12; 12; 12; 12; 12; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Bladder Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAUSTICUM 12 [hp_X]/1 SODIUM CHLORIDE 12 [hp_X]/1 STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/1 PULSATILLA VULGARIS WHOLE 12 [hp_X]/1 SEPIA OFFICINALIS JUICE 12 [hp_X]/1 DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/1 THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43689-0057-1 Bladder Relief 90 in 1 BOTTLE TABLET 90 2 43689-0057-2 Bladder Relief 1 in 1 PACKAGE TABLET 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43689-0057 BLADDER RELIEF (CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS) TABLET [THE MAGNI COMPANY] 2 Current NDC, Legacy NDC, 2 package rows 20240209_b09bf037-703f-4c22-8535-b33d586ebefa.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Bladder Relief CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS The Magni Company b09bf037-703f-4c22-8535-b33d586ebefa 2024-02-08 Warnings Exact identifier ndc (product): 43689-0057
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43689-0057-1 43689005701 90 in 1 BOTTLE Historical 43689-0057-2 43689005702 1 BOTTLE in 1 PACKAGE (43689-0057-2) / 90 TABLET in 1 BOTTLE (43689-0057-1) 1 bottle 2022-03-14 0000-00-00 No No Current