Multi-System
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2017-12-15
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:06:38
Label at a glance#
ProductMulti-System
Active ingredientUSTILAGO MAYDIS, ACONITUM NAPELLUS, ANTIMONY POTASSIUM TARTRATE, AMERICAN GINSENG, ARNICA MONTANA, ARSENIC TRIOXIDE, BAPTISIA TINCTORIA, BRYONIA ALBA ROOT, LYTTA VESICATORIA, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS BARK, ECHINACEA, UNSPECIFIED, IODINE, POTASSIUM CARBONATE, POTASSIUM IODIDE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, LYCOPUS VIRGINICUS, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PHYTOLACCA AMERICANA ROOT, PULSATILLA VULGARIS, TOXICODENDRON PUBESCENS LEAF, SAW PALMETTO, ASPERGILLUS NIGER VAR. NIGER, CLADOSPORIUM HERBARUM, CANDIDA ALBICANS, THYROID, UNSPECIFIED
Label structure10 sections
Contacts and useful links#
Websitewww.newtonlabs.net
www.newtonlabs.net
www.newtonlabs.netLabel contents#
Full prescribing information#
KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a doctor before use.
WARNINGS SECTION
Warning: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
QUESTIONS SECTION
www.newtonlabs.net Newton laboratories, Inc. FDA Est# 1051203 - Conyers, GA 30013. Questions? 1.800.448.7256
INACTIVE INGREDIENT SECTION
USP Purified water, USP Gluten-free, non-GMO, organic cane alcohol 20%.
PURPOSE SECTION
Formulated for symptoms associated with Valley Fever, Gulf War Syndrome, environmental sensitivity and other related conditions.
ACTIVE INGREDIENT SECTION
Equal parts of Aconitum nap. 10x, Antimonium tart. 10x, Aralia quinquefolia 10x, Arnica 10x, Arsenicum alb. 10x, Baptisia 10x, Bryonia 10x, Cantharis 10x, Chelidonium majus 10x, Cinchona 10x, Echinacea 10x, Iodum 10x, Kali carb. 10x, Kali iod. 10x, Lachesis 10x, Lycopodium 10x, Lycopus virginicus 10x, Nat. mur. 10x, Nux vom. 10x, Phosphorous 10x, Phytolacca 10x, Pulsatilla 10x, Rhus toxicodendron 10x, Sabal 10x, Allersodes 15x, Candida albicans 15x, Thyroidinum 15x, Ustilago maidis 15x.
DOSAGE & ADMINISTRATION SECTION
Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional.
INDICATIONS & USAGE SECTION
Formulated for symptoms associated with Valley Fever, Gulf War Syndrome, environmental sensitivity and other related conditions..
PACKAGE LABEL
Products#
Every source-derived product name is available through these pages.
- Multi-System
- Aspergillus niger, Cladosporium, Candida albicans, Thyroidinum, Ustilago maidis, Aconitum nap., Antimonium tart. Aralia quinquefolia, Arnica, Arsenicum alb., Baptisia, Bryonia, Cantharis, Chelidonium majus, Cinchona, Echinacea, Iodium, Kali carb. Kali iod., Lachesis, Lycopodium Lycopus virginicus, Nat. mur., Nux vom., Phosphorus, Phytolacca, Pulsatilla, Rhus toxicodendron, Sabal
- USTILAGO MAYDIS
- ACONITUM NAPELLUS
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- AMERICAN GINSENG
- ARNICA MONTANA
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- BAPTISIA TINCTORIA
- BRYONIA ALBA ROOT
- LYTTA VESICATORIA
- CHELIDONIUM MAJUS
- CINCHONA OFFICINALIS BARK
- ECHINACEA, UNSPECIFIED
- IODINE
- POTASSIUM CARBONATE
- CARBONATE ION
- POTASSIUM IODIDE
- IODIDE ION
- LACHESIS MUTA VENOM
- LYCOPODIUM CLAVATUM SPORE
- LYCOPUS VIRGINICUS
- SODIUM CHLORIDE
- CHLORIDE ION
- STRYCHNOS NUX-VOMICA SEED
- PHOSPHORUS
- PHYTOLACCA AMERICANA ROOT
- PULSATILLA VULGARIS
- TOXICODENDRON PUBESCENS LEAF
- SAW PALMETTO
- ALCOHOL
- ASPERGILLUS NIGER VAR. NIGER
- CLADOSPORIUM HERBARUM
- CANDIDA ALBICANS
- THYROID, UNSPECIFIED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-4638 | 55714-4638-1, 55714-4638-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 96c65757-bf34-72ea-e053-2995a90a2fd6 | 606569a1-be2d-4000-e053-2991aa0a04f5 | 2019-11-07 | Warnings | 606569a1-be2d-4000-e053-2991aa0a04f5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.