NDC product
NEORELIEF FOR MUSCLE CRAMPLING AND RESTLESSNESS
NDC 58368-002 · BioLyte Laboratories, LLC
Key facts
| Product NDC | 58368-002 |
|---|---|
| Proprietary name | NEORELIEF FOR MUSCLE CRAMPLING AND RESTLESSNESS |
| Nonproprietary name | topical gel for muscle cramping and restlessness |
| Substances | CAUSTICUM, JATROPHA CURCAS SEED, FRANGULA CALIFORNICA BARK, RUTA GRAVEOLENS FLOWERING TOP, ARNICA MONTANA, ATROPA BELLADONNA ROOT, BLACK COHOSH, ARTEMISIA CINA PRE-FLOWERING TOP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, HYPERICUM PERFORATUM, STRYCHNOS IGNATII SEED, POTASSIUM BROMIDE and 6 more |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | BioLyte Laboratories, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Feb 1, 2017 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: