Bladder Kidney Meridian Formula
- Product NDC
- 43742-0862
- Requested package NDC
- 43742-0862-1
- 11-digit product format
- 437420862
- Labeler code
- 43742
- Product ID
- 43742-0862_dfa96faa-6028-495e-b76a-df59f86105e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cinnamic Acid, Phloridzinum, Alpha-Ketoglutaricum Acidum, Ascorbic Acid, Kidney (Suis), Malicum Acidum, Nicotinamidum, Urinary Bladder (Suis), Adrenocorticotrophin, Apis Mellifica, Argentum Nitricum, Berberis Vulgaris, Cantharis, Equisetum Arvense, Kali Bichromicum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Phosphorus, Rhus Tox, Sepia, Terebinthina, Thuja Occidentalis, Dysentery Bacillus, Faecalis (Alkaligenes), Proteus (Vulgaris)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-10-04
- Marketing end
- 2022-07-24
- Substance
- CINNAMIC ACID; PHLORIZIN; OXOGLURIC ACID; ASCORBIC ACID; PORK KIDNEY; MALIC ACID; NIACINAMIDE; SUS SCROFA URINARY BLADDER; CORTICOTROPIN; APIS MELLIFERA; SILVER NITRATE; BERBERIS VULGARIS ROOT BARK; LYTTA VESICATORIA; EQUISETUM ARVENSE TOP; POTASSIUM DICHROMATE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; TURPENTINE OIL; THUJA OCCIDENTALIS LEAFY TWIG; SHIGELLA DYSENTERIAE; ALCALIGENES FAECALIS; PROTEUS VULGARIS
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 43742-0862 | 43742-0862-1 | D | Discontinued by firm | 2026-10-05 |
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.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43742-0862-1 | 43742086201 | 30 mL in 1 BOTTLE, DROPPER (43742-0862-1) | 30 ml | 2016-10-04 | 2022-07-24 | No | No | Current |