Veive CBD Pain and Cramps
- Product NDC
- 58368-013
- Requested package NDC
- 58368-013-01
- 11-digit product format
- 583680013
- Labeler code
- 58368
- Product ID
- 58368-013_d086d2f8-9302-e60d-e053-2995a90a2004
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Apis Mellifica, Arnica Montana, Belladonna, Bryonia Alba, Cimicifuga Racemosa, Cyclymen Europaeum, Joanesia Asoca, Kali Carbonicum, Lilium Tigrinum, Rhamnus Californica, Sabina Bellis Perennis, Cactus Grandiflorus, Caulophyllum Thalictroides, Colocynthis, Gelsemium Sempervirens, Viburnum Opulus, Tilia Europaea
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BioLyte Laboratories, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-11-16
- Marketing end
- 0000-00-00
- Substance
- BRYONIA ALBA ROOT; SARACA INDICA BARK; ATROPA BELLADONNA; CAULOPHYLLUM THALICTROIDES ROOT; SELENICEREUS GRANDIFLORUS STEM; JUNIPERUS SABINA LEAFY TWIG; APIS MELLIFERA; ARNICA MONTANA; CYCLAMEN PURPURASCENS TUBER; POTASSIUM CARBONATE; LILIUM LANCIFOLIUM WHOLE FLOWERING; BLACK COHOSH; CITRULLUS COLOCYNTHIS FRUIT PULP; GELSEMIUM SEMPERVIRENS ROOT; TILIA X EUROPAEA FLOWER; VIBURNUM OPULUS BARK; FRANGULA CALIFORNICA BARK; BELLIS PERENNIS
- 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 | 58368-013 | 58368-013-01 | 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 |
|---|---|---|---|---|---|---|---|---|
| 58368-013-01 | 58368001301 | 5 g in 1 PACKET (58368-013-01) | 5 g | 2020-11-16 | 0000-00-00 | Yes | No | Current |