Dosage and administration
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Systemic Detox
- Manufacturer
- Deseret Biologicals, Inc. | Apotheca Company
- Effective date
- 2021-01-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:55:56
Label at a glance#
ProductSystemic Detox
Active ingredientBETA VULGARIS, PEUMUS BOLDUS LEAF, CHELIDONIUM MAJUS, SMILAX ARISTOLOCHIIFOLIA ROOT, GELSEMIUM SEMPERVIRENS ROOT, VERATRUM ALBUM ROOT, IRON, IODINE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, ANEMONE PRATENSIS, SELENIUM, THUJA OCCIDENTALIS LEAFY TWIG, ZINC
Label structure9 sections
Contacts and useful links#
Websitewww.desbio.com
www.desbio.com
www.desbio.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Beta Vulgaris 3X, Boldo 3X, Chelidonium Majus 3X, Sarsaparilla (Smilax Medica) 6X, Gelsemium Sempervirens 8X, Veratrum Album 8X, Ferrum Metallicum 12X, Iodium 12X, Lycopodium Clavatum 12X, Nux Vomica 12X, Pulsatilla (Pratensis) 12X, Selenium Metallicum 12X, Thuja Occidentalis 12X, Zincum Metallicum 12X.
HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to excretory dysfunction including mucous congestion.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
WARNINGS:
Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use.
Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.
DIRECTIONS:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to excretory dysfunction including mucous congestion.**
**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INACTIVE INGREDIENTS:
Demineralized Water, 25% Ethanol
QUESTIONS:
PACKAGE LABEL DISPLAY:
DESBIO
NDC 43742-1555-1
HOMEOPATHIC
SYSTEMIC
DRAINAGE
1 FL OZ (30 ml)
Products#
Every source-derived product name is available through these pages.
- Systemic Detox
- Beta Vulgaris, Boldo, Chelidonium Majus, Sarsaparilla (Smilax Medica), Gelsemium Sempervirens, Veratrum Album, Ferrum Metallicum, Iodium, Lycopodium Clavatum, Nux Vomica, Pulsatilla (Pratensis), Selenium Metallicum, Thuja Occidentalis, Zincum Metallicum
- BETA VULGARIS
- PEUMUS BOLDUS LEAF
- CHELIDONIUM MAJUS
- SMILAX ARISTOLOCHIIFOLIA ROOT
- GELSEMIUM SEMPERVIRENS ROOT
- VERATRUM ALBUM ROOT
- IRON
- IODINE
- LYCOPODIUM CLAVATUM SPORE
- STRYCHNOS NUX-VOMICA SEED
- ANEMONE PRATENSIS
- SELENIUM
- THUJA OCCIDENTALIS LEAFY TWIG
- ZINC
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43742-1555 | 43742-1555-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BETA VULGARIS | 4G174V5051 | ACTIB |
| PEUMUS BOLDUS LEAF | Q4EWM09M3O | ACTIB |
| CHELIDONIUM MAJUS | 7E889U5RNN | ACTIB |
| SMILAX ARISTOLOCHIIFOLIA ROOT | NR100Y25G0 | ACTIB |
| GELSEMIUM SEMPERVIRENS ROOT | 639KR60Q1Q | ACTIB |
| VERATRUM ALBUM ROOT | QNS6W5US1Z | ACTIB |
| IRON | E1UOL152H7 | ACTIB |
| IODINE | 9679TC07X4 | ACTIB |
| LYCOPODIUM CLAVATUM SPORE | C88X29Y479 | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| ANEMONE PRATENSIS | 8E272251DI | ACTIB |
| SELENIUM | H6241UJ22B | ACTIB |
| THUJA OCCIDENTALIS LEAFY TWIG | 1NT28V9397 | ACTIB |
| ZINC | J41CSQ7QDS | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 0c1fe331-8dd8-478e-be44-0c709289a11a | ca4e4985-051c-4b84-bc54-accedeb91cfe | 2021-01-20 | Warnings | 0c1fe331-8dd8-478e-be44-0c709289a11a ca4e4985-051c-4b84-bc54-accedeb91cfe |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.