BronCare
- Product NDC
- 55714-4777
- Requested package NDC
- 55714-4777-1
- 11-digit product format
- 557144777
- Labeler code
- 55714
- Product ID
- 55714-4777_b9fca640-72f0-5bd4-e053-2995a90ab623
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea, Lappa, Rumex crisp., Antimon. tart., Arsenicum alb., Bryonia, Camphora, Chelidonium maj., Cinchona, Drosera, Eucalyptus, Hepar sulph. calc., Histaminum hydrochloricum, Ipecac., Kali bic., Kali carb., Kali iod., Lycopodium, Myrrha, Nat. sulphuricum, Nux vom., Phos., Pulsatilla, Sainguinaria, Spongia, Stannum met., Tussilago far., Verbascum, Influenzinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Newton Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-09-02
- Marketing end
- 0000-00-00
- Substance
- CINCHONA OFFICINALIS BARK; CALCIUM SULFIDE; HISTAMINE DIHYDROCHLORIDE; IPECAC; ARCTIUM LAPPA ROOT; INFLUENZA A VIRUS; ANEMONE PULSATILLA; DROSERA ANGLICA; LYCOPODIUM CLAVATUM SPORE; SODIUM SULFATE; RUMEX CRISPUS ROOT; ANTIMONY POTASSIUM TARTRATE; EUCALYPTUS GUM; POTASSIUM IODIDE; ARSENIC TRIOXIDE; CAMPHOR (NATURAL); ECHINACEA, UNSPECIFIED; POTASSIUM CARBONATE; MYRRH; PHOSPHORUS; VERBASCUM THAPSUS; POTASSIUM DICHROMATE; BRYONIA ALBA ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED; TUSSILAGO FARFARA; CHELIDONIUM MAJUS; TIN; INFLUENZA B VIRUS; STRYCHNOS NUX-VOMICA SEED; SANGUINARIA CANADENSIS ROOT
- Active strength
- 15 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 55714-4777 | 55714-4777-1 | D | Discontinued by firm | 2026-10-15 |
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 |
|---|---|---|---|---|---|---|---|---|
| 55714-4777-1 | 55714477701 | 28 g in 1 BOTTLE, GLASS (55714-4777-1) | 28 g | 2019-09-02 | 0000-00-00 | No | No | Current |