Heart Small Intestine Meridian Formula
- Product NDC
- 43742-0690
- Requested package NDC
- 43742-0690-1
- 11-digit product format
- 437420690
- Labeler code
- 43742
- Product ID
- 43742-0690_bec72f08-cb2e-4a4d-9eee-e6715a8cc771
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adrenlinum, Coumarinum, Tyramine, Arteria Suis, Ascorbic Acid, Cactus Grandiflorus, Coenzyme A, Glonoinum, Heart (Suis), Sarcolacticum Acidum, Ubidecarenonum, Vein (Suis), Adrenocorticotrophin, Arsenicum Album, Aurum Metallicum, Belladonna, Digitalis Purpurea, Kali Carbonicum, Lithium Carbonicum, Lycopodium Clavatum, Mercurius Solubilis, Naja Tripudians, Nux Vomica, Phosphorus, Pulsatilla (Vulgaris), Spigelia Anthelmia, Dysentery Bacillus, Gaertner Bacillus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-12-08
- Marketing end
- 2021-03-25
- Substance
- EPINEPHRINE; COUMARIN; TYRAMINE; SUS SCROFA ARTERY; ASCORBIC ACID; SELENICEREUS GRANDIFLORUS STEM; COENZYME A; NITROGLYCERIN; PORK HEART; LACTIC ACID, L-; UBIDECARENONE; SUS SCROFA VEIN; CORTICOTROPIN; ARSENIC TRIOXIDE; GOLD; ATROPA BELLADONNA; DIGITALIS; POTASSIUM CARBONATE; LITHIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; NAJA NAJA VENOM; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; PULSATILLA VULGARIS; SPIGELIA ANTHELMIA; SHIGELLA DYSENTERIAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS
- Active strength
- 6 [hp_X]/mL; [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; [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 | 43742-0690 | 43742-0690-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 43742-0690-1 | 43742069001 | 30 mL in 1 BOTTLE, DROPPER (43742-0690-1) | 30 ml | 2015-12-08 | 2021-03-25 | No | No | Current |