NDC product
Bladder Relief
NDC 43689-0057 · The Magni Company
Key facts
| Product NDC | 43689-0057 |
|---|---|
| Proprietary name | Bladder Relief |
| Nonproprietary name | Causticum, Natrum Muriaticum, Nux Vomica, Pulsatilla (Vulgaris), Sepia, Staphysagria, Thuja Occidentalis |
| Substances | CAUSTICUM, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS WHOLE, SEPIA OFFICINALIS JUICE, DELPHINIUM STAPHISAGRIA SEED, THUJA OCCIDENTALIS LEAFY TWIG |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | The Magni Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| Marketing start | Mar 14, 2022 |
| Listing certified through | Dec 31, 2026 |
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: