Hevert Cough Relief
- Product NDC
- 54532-0015
- Requested package NDC
- 54532-0015-4
- 11-digit product format
- 545320015
- Labeler code
- 54532
- Product ID
- 54532-0015_8773280c-e0fc-465c-b71c-9de935e67d75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- drosera rotundifolia, drosera intermedia, drosera anglica, eriodictyon californicum flowering top, grindelia hirsutula flowering top, potassium iodide, spongia officinalis skeleton, roasted, lobaria pulmonaria, teucrium scorodonia flowering top, and verbascum densiflorum flowering top
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hevert Arzneimittel GmbH & Co KG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-03-07
- Marketing end
- 0000-00-00
- Substance
- DROSERA ANGLICA WHOLE; DROSERA INTERMEDIA WHOLE; DROSERA ROTUNDIFOLIA WHOLE; ERIODICTYON CALIFORNICUM FLOWERING TOP; GRINDELIA HIRSUTULA FLOWERING TOP; LOBARIA PULMONARIA; POTASSIUM IODIDE; SPONGIA OFFICINALIS SKELETON, ROASTED; TEUCRIUM SCORODONIA FLOWERING TOP; VERBASCUM DENSIFLORUM FLOWERING TOP
- Active strength
- 4 [hp_X]/1; [hp_X]/1; [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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 54532-0015 | 54532-0015-4 | 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.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 54532-0015-4 | 54532001504 | 10 BLISTER PACK in 1 CARTON (54532-0015-4) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2013-03-07 | 0000-00-00 | No | No | Current |