Hayfever Tonic
- Product NDC
- 43857-0441
- Requested package NDC
- 43857-0441-1
- 11-digit product format
- 438570441
- Labeler code
- 43857
- Product ID
- 43857-0441_04072341-05b6-48bf-b60d-ec3d8a4623fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea Purpurea, Hydrastis Canadensis, Eupatorium Perfoliatum, Verbascum Thapsus, Alfalfa, American Elm, Platanus, Fraxinus Americana, Fagus Sylvatica, Flos, Black Walnut, Salix Nigra, Negundo, Eastern Cottonwood, False Ragweed, Giant Ragweed, Solidago Virguarea, Kentucky Bluegrass, Orchard Grass, Red Birch, Trifolium Pratense, Red Oak, Redtop Grass, Hickory, Rumex Acetosa, Ambrosia Artemesiafolia, Timothy Grass, Western Ragweed, Rumex Crispus, Ailanthus Glandulosus, Allium Cepa, Aurum Muriaticum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-05-17
- Marketing end
- 2022-05-16
- Substance
- ECHINACEA PURPUREA; EUPATORIUM PERFOLIATUM FLOWERING TOP; VERBASCUM THAPSUS; GOLDENSEAL; ALFALFA; ULMUS AMERICANA POLLEN; ACER PSEUDOPLATANUS POLLEN; FRAXINUS AMERICANA POLLEN; FAGUS SYLVATICA FLOWERING TOP; JUGLANS NIGRA POLLEN; SALIX NIGRA POLLEN; ACER NEGUNDO POLLEN; POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN; AMBROSIA ACANTHICARPA POLLEN; AMBROSIA TRIFIDA POLLEN; SOLIDAGO VIRGAUREA POLLEN; POA PRATENSIS POLLEN; DACTYLIS GLOMERATA POLLEN; BETULA OCCIDENTALIS POLLEN; TRIFOLIUM PRATENSE POLLEN; QUERCUS RUBRA POLLEN; AGROSTIS GIGANTEA POLLEN; CARYA OVATA POLLEN; RUMEX ACETOSELLA POLLEN; AMBROSIA ARTEMISIIFOLIA POLLEN; PHLEUM PRATENSE POLLEN; AMBROSIA PSILOSTACHYA POLLEN; RUMEX CRISPUS POLLEN; AILANTHUS ALTISSIMA POLLEN; ONION; GOLD TRICHLORIDE; CAMPHOR (NATURAL); IPECAC; POTASSIUM DICHROMATE; SOLIDAGO VIRGAUREA FLOWERING TOP
- Active strength
- 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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 | 43857-0441 | 43857-0441-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 43857-0441-1 | 43857044101 | 60 mL in 1 BOTTLE, DROPPER (43857-0441-1) | 60 ml | 2017-05-17 | 2022-05-16 | No | No | Current |