Trauma Remedy
- Product NDC
- 43742-0172
- Requested package NDC
- 43742-0172-1
- 11-digit product format
- 437420172
- Labeler code
- 43742
- Product ID
- 43742-0172_d76c09d0-d17b-483e-bbd0-9d3636a15264
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chamomilla, Echinacea (Angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia (Alba), Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Rhus Tox, Clematis Vitalba flos, Helianthemum Nummularium flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera flos, Ornithogalum Umbellatum flos, Prunus Cerasifera flos, Carbo Vegetabilis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-31
- Marketing end
- 2021-06-23
- Substance
- ECHINACEA ANGUSTIFOLIA; MATRICARIA RECUTITA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; ARNICA MONTANA; ATROPA BELLADONNA; BELLIS PERENNIS; TOXICODENDRON PUBESCENS LEAF; CLEMATIS VITALBA FLOWER; HELIANTHEMUM NUMMULARIUM FLOWER; CALCIUM SULFIDE; IMPATIENS GLANDULIFERA FLOWER; ORNITHOGALUM UMBELLATUM FLOWERING TOP; PRUNUS CERASIFERA FLOWER; ACTIVATED CHARCOAL
- Active strength
- 3 [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 | 43742-0172 | 43742-0172-1 | 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.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43742-0172-1 | 43742017201 | 30 mL in 1 BOTTLE, DROPPER (43742-0172-1) | 30 ml | 2015-10-14 | 2021-06-23 | No | No | Current |