HAIR STIM
- Product NDC
- 50181-0053
- Requested package NDC
- 50181-0053-1
- 11-digit product format
- 501810053
- Labeler code
- 50181
- Product ID
- 50181-0053_6fe987e5-890b-4901-ad15-8adaf8138711
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pediculus Capitis, Thyroidinum (Suis), Baryta Carbonica, Borax, Calcarea Carbonica, Cinchona Officinalis, Glandula Suprarenalis Suis, Hydrofluoricum Acidum, Mercurius Solubilis, Mezereum, Natrum Muriaticum, Phosphorus, Pulsatilla (Pratensis), Sepia, Silicea, Sulphur, Thuja Occidentalis, Vinca Minor
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-22
- Marketing end
- 2022-04-18
- Substance
- PEDICULUS HUMANUS VAR. CAPITIS; THYROID, PORCINE; BARIUM CARBONATE; SODIUM BORATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CINCHONA OFFICINALIS BARK; SUS SCROFA ADRENAL GLAND; HYDROFLUORIC ACID; MERCURIUS SOLUBILIS; DAPHNE MEZEREUM BARK; SODIUM CHLORIDE; PHOSPHORUS; PULSATILLA PRATENSIS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; VINCA MINOR
- Active strength
- 4 [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
- 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 | 50181-0053 | 50181-0053-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 50181-0053-1 | 50181005301 | 30 mL in 1 BOTTLE, SPRAY (50181-0053-1) | 30 ml | 2017-05-04 | 2022-04-18 | No | No | Current |