Sick Stopper

Manufacturer
Newton Laboratories, Inc.
Effective date
2020-01-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:43:46

Label at a glance#

ProductSick Stopper
Active ingredientECHINACEA, UNSPECIFIED, AMERICAN GINSENG, BAPTISIA TINCTORIA ROOT, BRYONIA ALBA ROOT, CHELIDONIUM MAJUS, EUPATORIUM PERFOLIATUM FLOWERING TOP, CALCIUM SULFIDE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG, BUFO BUFO CUTANEOUS GLAND, STRYCHNOS NUX-VOMICA SEED, BACILLUS ANTHRACIS IMMUNOSERUM RABBIT, INFLUENZA A VIRUS, INFLUENZA B VIRUS, RANCID BEEF, ACONITUM NAPELLUS, AMANITA MUSCARIA FRUITING BODY
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with colds and infections. Begin at the onset of symptoms.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Echinacea 6x, Aconitum napellus 10x, Agaricus muscarius 10x, Aralia quinquefolia 10x, Baptisia tinctoria 10x, Bryonia 10x, Chelidonium majus 10x, Eupatorium perfoliatum 10x, Hepar sulphuris calcareum 10x, Lachesis mutus 10x, Lycopodium clavatum 10x, Rhus toxicodendron 10x, Sanguinaria canadensis 10x, Sulphur 10x, Thuja occidentalis 10x, Bufo rana 15x, Nux vomica 15x, Anthracinum 30x, Influenzinum 30x, Pyrogenium 30x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with colds and infections. Begin at the onset of symptoms.

INACTIVE INGREDIENT SECTION

Active Ingredients: Gluten-free, non-GMO, organic beet-derived sucrose (lactose-free) pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: 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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets by mouth (ages 0 to 11, give 3 pellets) as need or as directed by a health professional. Under age 2, crush/dissolve pellets in purified water. Sensitive person begin with 1 drop and gradually increase to full dose.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-251755714-2517-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b56be0cc-103a-421d-e053-2995a90ac91e9cc2c9d2-9c8f-338e-e053-2a95a90a23622020-12-01WarningsExact identifier
spl set id: 9cc2c9d2-9c8f-338e-e053-2a95a90a2362

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.