Veive CBD Muscle Relaxer
- Product NDC
- 58368-012
- Requested package NDC
- 58368-012-01
- 11-digit product format
- 583680012
- Labeler code
- 58368
- Product ID
- 58368-012_d086d571-760b-668d-e053-2995a90a6921
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Montana, Causticum, Rhamnus Californica, Ruta Graveolens, Taraxacum Officinale, Belladonna, Cimicifuga Racemosa, Gnaphalium Polycephalum, Hypericum Perforatum, Jatropha Curcas, Veratrum Album, Cina, Ignatia Amara, Kali Bromatum, Kali Carbonicum, Lycopodium Clavatum, Scutellaria Lateriflora, Valeriana Officinalis
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BioLyte Laboratories, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-11-16
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA; STRYCHNOS IGNATII SEED; RUTA GRAVEOLENS FLOWERING TOP; SCUTELLARIA LATERIFLORA WHOLE; TARAXACUM OFFICINALE; VALERIAN; VERATRUM ALBUM ROOT; ATROPA BELLADONNA; CAUSTICUM; ARTEMISIA CINA FLOWER; POTASSIUM BROMIDE; POTASSIUM CARBONATE; FRANGULA CALIFORNICA BARK; HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; BLACK COHOSH; PSEUDOGNAPHALIUM OBTUSIFOLIUM; JATROPHA CURCAS SEED
- Active strength
- 4 [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 | 58368-012 | 58368-012-01 | 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 |
|---|---|---|---|---|---|---|---|---|
| 58368-012-01 | 58368001201 | 5 g in 1 PACKET (58368-012-01) | 5 g | 2020-11-16 | 0000-00-00 | Yes | No | Current |