Sick Stopper

Manufacturer
Newton Laboratories, Inc.
Effective date
2011-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:05:03

Label at a glance#

ProductSick Stopper
Active ingredientBacillus Anthracis Immunoserum Rabbit, Influenza A Virus, Rancid Beef, Bufo Bufo Cutaneous Gland, Aconitum Napellus, Amanita Muscaria Var. Muscaria Fruiting Body, American Ginseng, Baptisia Tinctoria, Bryonia Alba Root, Chelidonium Majus, Eupatorium Perfoliatum Flowering Top, Calcium Sulfide, Lachesis Muta Venom, Lycopodium Clavatum Spore, Strychnos Nux-vomica Seed, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur, Thuja Occidentalis Leafy Twig, Echinacea, Unspecified, Influenza B Virus
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions:   Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) as needed or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water.  Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Anthracinum 30x, Influenzinum 30x, Pyrogenium 30x, Bufo rana 15x, Aconitum nap. 10x, Agaricus musc. 10x, Aralia quinquefolia 10x, Baptisia 10x, Bryonia 10x, Chelidonium majus 10x, Eupatorium perf. 10x, Hepar sulph. calc. 10x, Lachesis 10x, Lycopodium 10x, Nux vom. 10x, Rhus toxicodendron 10x, Sanguinaria 10x, Sulphur 10x, Thuja occ. 10x, Echinacea 3x.

OTC - PURPOSE SECTION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions?  1.800.448.7256 

WARNINGS SECTION

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.  

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55714-1114-02020-01-31C16284748780-19d75b9d0-5764-f424-e053-dadaa90a57ceSick Stopper
55714-1114-12020-01-31C16284748780-19d75b9d0-5764-f424-e053-dadaa90a57ceSick Stopper
55714-1114-22020-01-31C16284748780-19d75b9d0-5764-f424-e053-dadaa90a57ceSick Stopper

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-1114SICK STOPPER (ANTHRACINUM, INFLUENZA A VIRUS, INFLUENZA B VIRUS, PYROGENIUM, BUFO RANA, ACONITUM NAP., AGARICUS MUSC., ARALIA QUINQUEFOLIA, BAPTISIA, BRYONIA, CHELIDONIUM MAJUS, EUPATORIUM PERF., HEPAR SULPH. CALC., LACHESIS, LYCOPODIUM, NUX VOM., RHUS TOXICODENDRON, SANGUINARIA, SULPHUR, THUJA OCC., ECHINACEA) PELLET [NEWTON LABORATORIES, INC.]1Legacy NDC20131018_6b12b072-1d0e-17c7-dbe4-b2b294e14aca.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aconitum NapellusACTIVE INGREDIENTU0NQ8555JD1
Amanita Muscaria Var. Muscaria Fruiting BodyACTIVE INGREDIENTDIF093I0371
American GinsengACTIVE INGREDIENT8W75VCV53Q1
Bacillus Anthracis Immunoserum RabbitACTIVE INGREDIENT41LZ22DD4N1
Baptisia TinctoriaACTIVE INGREDIENT5K1UO2888Y1
Bryonia Alba RootACTIVE INGREDIENTT7J046YI2B1
Bufo Bufo Cutaneous GlandACTIVE INGREDIENTQ59QU6N72Q1
Calcium SulfideACTIVE INGREDIENT1MBW07J51Q1
Chelidonium MajusACTIVE INGREDIENT7E889U5RNN1
Echinacea, UnspecifiedACTIVE INGREDIENT4N9P6CC1DX1
Eupatorium Perfoliatum Flowering TopACTIVE INGREDIENT1W0775VX6E1
Influenza A VirusACTIVE INGREDIENTR9HH0NDE2E1
Influenza B VirusACTIVE INGREDIENT1314JZ2X6W1
Lachesis Muta VenomACTIVE INGREDIENTVSW71SS07I1
Lycopodium Clavatum SporeACTIVE INGREDIENTC88X29Y4791
Rancid BeefACTIVE INGREDIENT29SUH5R3HU1
Sanguinaria Canadensis RootACTIVE INGREDIENTN9288CD5081
Strychnos Nux-vomica SeedACTIVE INGREDIENT269XH139191
SulfurACTIVE INGREDIENT70FD1KFU701
Thuja Occidentalis Leafy TwigACTIVE INGREDIENT1NT28V93971
Toxicodendron Pubescens LeafACTIVE INGREDIENT6IO182RP7A1
Aconitum NapellusACTIVE MOIETYU0NQ8555JD1
Amanita Muscaria Var. Muscaria Fruiting BodyACTIVE MOIETYDIF093I0371
American GinsengACTIVE MOIETY8W75VCV53Q1
Bacillus Anthracis Immunoserum RabbitACTIVE MOIETY41LZ22DD4N1
Baptisia TinctoriaACTIVE MOIETY5K1UO2888Y1
Bryonia Alba RootACTIVE MOIETYT7J046YI2B1
Bufo Bufo Cutaneous GlandACTIVE MOIETYQ59QU6N72Q1
Calcium SulfideACTIVE MOIETY1MBW07J51Q1
Chelidonium MajusACTIVE MOIETY7E889U5RNN1
Echinacea, UnspecifiedACTIVE MOIETY4N9P6CC1DX1
Eupatorium Perfoliatum Flowering TopACTIVE MOIETY1W0775VX6E1
Influenza A VirusACTIVE MOIETYR9HH0NDE2E1
Influenza B VirusACTIVE MOIETY1314JZ2X6W1
Lachesis Muta VenomACTIVE MOIETYVSW71SS07I1
Lycopodium Clavatum SporeACTIVE MOIETYC88X29Y4791
Rancid BeefACTIVE MOIETY29SUH5R3HU1
Sanguinaria Canadensis RootACTIVE MOIETYN9288CD5081
Strychnos Nux-vomica SeedACTIVE MOIETY269XH139191
SulfurACTIVE MOIETY70FD1KFU701
Thuja Occidentalis Leafy TwigACTIVE MOIETY1NT28V93971
Toxicodendron Pubescens LeafACTIVE MOIETY6IO182RP7A1
SucroseINACTIVE INGREDIENTC151H8M5541

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-111455714-1114-1, 55714-1114-2, 55714-1114-0

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

Inactive ingredient matches#

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.

Inactive ingredient links page 1 of 1 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS308 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CONCENTRATE / ORAL4800 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SOLUTION / ORAL38666 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / SUBCUTANEOUS47.75 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, DELAYED RELEASE / ORAL295.33 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554PASTILLE / ORAL426 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED PELLETS / ORAL59.8 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554DROPS / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION / ORAL48209 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTABLE, LIPOSOMAL / INTRAVENOUS7560 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED / ORAL145 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED, EXTENDED RELEASE / ORAL119.12 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SOLUTION / INTRAVENOUSNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS2000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, EMULSION / INTRAVENOUS970 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / BUCCAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554WAFER / ORAL155.2 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, EXTENDED RELEASE / ORAL619 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, CHEWABLE / ORAL7258 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS1 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554ELIXIR / ORAL18000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION, EXTENDED RELEASE / ORAL5400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED, EXTENDED RELEASE / ORAL86 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / ORAL4249 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS900 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, COATED / ORAL516.42 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SOLUTION / ORAL42596 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE / ORAL3568 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL18790 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / RECTAL35.42 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION / ORAL31885 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / TRANSMUCOSAL1255 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, DELAYED RELEASE / ORAL955 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / INTRAVENOUS1950 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, EXTENDED RELEASE / ORAL284.54 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii candidate
48 equally ranked IID candidates

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
40819069-1bce-5116-e063-6394a90afd3c6b12b072-1d0e-17c7-dbe4-b2b294e14aca2025-10-06WarningsExact identifier
spl set id: 6b12b072-1d0e-17c7-dbe4-b2b294e14aca

Reported adverse events (FAERS/openFDA)#

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