Dosage and administration
1 drop under tongue or as directed by a health practitioner. Consult a physician for use in children under 12 years of age.
1 drop under tongue or as directed by a health practitioner. Consult a physician for use in children under 12 years of age.
Fucus Vesiculosus 3X, Thyroidinum 6X, 30C, Spongia Tosta 12X.
Formulated for symptoms such as sluggish metabolism, weight gain, fatigue, and hair loss.
If pregnant or breast-feeding, 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.
Do not use if tamper evident seal is broken or missing.
Store in a cool, dry place.
1 drop under tongue or as directed by a health practitioner. Consult a physician for use in children under 12 years of age.
Demineralized Water, 20% Ethanol, Glycerin, Kelp (Whole Plant) (Laminaria spp.) Extract, Potassium Iodide USP, Sodium Iodide USP.
In case of overdose, get medical help or contact a Poison Control Center right away.
Formulated for symptoms such as sluggish metabolism, weight gain, fatigue, and hair loss.
Proprietary Blend for Institute for Wholistic Rejuvenation.
Dist. by: Institute for Wholistic
Rejuvenation, Sandpoint, ID 83864
(888) 352.8175
WHOLISTIC
THYROID
BALANCE
HOMEOPATHIC
INSTITUTE FOR
WHOLISTIC
REJUVENATION
1 fl. oz. (30 ml)
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0640522597802 | GTIN-13: 0640522597802 EAN-13: 0640522597802 GTIN-12: 640522597802 UPC-A: 640522597802 GTIN storage (14 digits): 00640522597802 | ENRGGLGL0237 Wholistic Thyroid Balance 1-3-23.jpg |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| FUCUS VESICULOSUS | ACTIVE INGREDIENT | 535G2ABX9M | 2 | |
| SPONGIA OFFICINALIS SKELETON, ROASTED | ACTIVE INGREDIENT | 1PIP394IID | 2 | |
| SUS SCROFA THYROID | ACTIVE INGREDIENT | 6RV024OAUQ | 2 | |
| FUCUS VESICULOSUS | ACTIVE MOIETY | 535G2ABX9M | 2 | |
| SPONGIA OFFICINALIS SKELETON, ROASTED | ACTIVE MOIETY | 1PIP394IID | 2 | |
| SUS SCROFA THYROID | ACTIVE MOIETY | 6RV024OAUQ | 2 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 2 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | 2 | |
| LAMINARIA DIGITATA | INACTIVE INGREDIENT | 15E7C67EE8 | 2 | |
| POTASSIUM IODIDE | INACTIVE INGREDIENT | 1C4QK22F9J | 2 | |
| SODIUM IODIDE | INACTIVE INGREDIENT | F5WR8N145C | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 55330-0001 | 55330-0001-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FUCUS VESICULOSUS | 535G2ABX9M | ACTIB |
| SUS SCROFA THYROID | 6RV024OAUQ | ACTIB |
| SPONGIA OFFICINALIS SKELETON, ROASTED | 1PIP394IID | ACTIB |
| SODIUM IODIDE | F5WR8N145C | IACT |
| POTASSIUM IODIDE | 1C4QK22F9J | IACT |
| LAMINARIA DIGITATA | 15E7C67EE8 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 6 | 2023-04-03 | full-release | 2026-06-01 02:20:44 |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | DOUCHE / VAGINAL | 0.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | SPONGE / TOPICAL | 0.74 %w/w | ||
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | INJECTION / INTRAVENOUS | 10 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | LIQUID / ORAL | 2400 mg | ||
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | INJECTION / INTRAVENOUS | 10 mg | ||
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | SPONGE / TOPICAL | 0.74 %w/w | ||
| SODIUM IODIDE | SODIUM IODIDE | F5WR8N145C | DOUCHE / VAGINAL | 0.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| GLYCERIN | GLYCERIN | PDC6A3C0OX | LIQUID / ORAL | 2400 mg |
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 |
|---|---|---|---|---|---|---|
| 4c37603e-04de-4269-b6d6-d53234b5c89c | b45aa21e-1a4b-4589-8687-e41a52f527dc | 2023-04-03 | Warnings | b45aa21e-1a4b-4589-8687-e41a52f527dc |
Adverse event summaries are temporarily unavailable. Other product information remains available.