Indications and uses
For the temporary relief of urinary frequency
For the temporary relief of urinary frequency
• Adults and children 12 years and above, dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician • Children under 12 years, consult a physician • Take at least 10 minutes before or after eating or drinking
Causticum 12X, Natrum Muriaticum 12X, Nux Vomica 12X, Pulsatilla (Vulgaris) 12X, Sepia 12X, Staphysagria 12X, Thuja Occidentalis 12X.
For the temporary relief of urinary frequency
• If pregnant or breastfeeding, ask a health professional before use
• Keep out of reach of children • In case of overdose, get medical help or contact a Poison Control Center right away
• Stop use and ask a doctor if symptoms persist for more than 7 days or worsen, or if you have symptoms of a urinary tract infection
• Store tightly closed in a dry place
• Tamper sealed: Sealed for your protection. Do not use if seal is broken or missing
• The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United
States
• These statements are supported by the traditional homeopathic principles
In case of overdose, get medical help or contact a Poison Control Center right away
• Adults and children 12 years and above, dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician
• Children under 12 years, consult a physician
• Take at least 10 minutes before or after eating or drinking
For the temporary relief of urinary frequency
Lactose, Magnesium Stearate, Microcrystalline Cellulose
Dist. by: The Magni Group, Inc. McKinney, TX 75071 USA
www.magilife.com 1-800-645-9199
MAGNILIFE Homeopathic
BLADDER NDC 43689-0057-1
RELIEF
For the temporary relief
of urinary frequency
√ Overactive Bladder
√ Urinary Frequency
90 Tablets
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43689-0057-2 | 2024-02-08 | C162847 | 48780-1 | 1030e365-63ed-111a-e063-dadaa90a10e2 | DRUG FACTS: |
| 43689-0057-2 | 2024-01-30 | C162847 | 48780-1 | 1030e365-63ed-111a-e063-dadaa90a10e2 | DRUG FACTS: |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43689-0057-1 | Bladder Relief | 90 in 1 BOTTLE | TABLET | 90 | 2 | |
| 43689-0057-2 | Bladder Relief | 1 in 1 PACKAGE | TABLET | 1 | 2 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43689-0057 | BLADDER RELIEF (CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS) TABLET [THE MAGNI COMPANY] | 2 | Current NDC, Legacy NDC, 2 package rows | 20240209_b09bf037-703f-4c22-8535-b33d586ebefa.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 43689-0057 | 43689-0057-1, 43689-0057-2 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CAUSTICUM | DD5FO1WKFU | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| PULSATILLA VULGARIS WHOLE | I76KB35JEV | ACTIB |
| SEPIA OFFICINALIS JUICE | QDL83WN8C2 | ACTIB |
| DELPHINIUM STAPHISAGRIA SEED | 00543AP1JV | ACTIB |
| THUJA OCCIDENTALIS LEAFY TWIG | 1NT28V9397 | ACTIB |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| CELLULOSE, MICROCRYSTALLINE | OP1R32D61U | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Bladder Relief | CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS | The Magni Company | b09bf037-703f-4c22-8535-b33d586ebefa | 2024-02-08 | Warnings | 43689-0057-1 43689-0057-2 43689-0057 43689005701 43689005702 ce5b0b46-200c-4aad-a550-fb965099721a b09bf037-703f-4c22-8535-b33d586ebefa |
Adverse event summaries are temporarily unavailable. Other product information remains available.