Urinary Incontinence Relief
- Product NDC
- 43689-0001
- 11-digit product format
- 436890001
- Labeler code
- 43689
- Product ID
- 43689-0001_c75a0e09-69d7-4ffd-8f84-ec61cf866718
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Causticum, Natrum muriaticum, Nus vomica, Pulsatilla, Sepia, Staphysagria, Thuja occidentalis,
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Magni Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-07-17
- Marketing end
- 2023-01-11
- Substance
- CAUSTICUM; DELPHINIUM STAPHISAGRIA SEED; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 12 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43689-0001-1 | 43689000101 | 125 TABLET in 1 BOTTLE (43689-0001-1) | 125 tablet | 2012-07-17 | 2023-01-11 | No | No | Current |