Throat Care

Manufacturer
Newton Laboratories, Inc.
Effective date
2011-03-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:05:00

Label at a glance#

ProductThroat Care
Active ingredientAconitum Napellus, Apis Mellifera, Arisaema Dracontium Root, Atropa Belladonna, Bryonia Alba Root, Cajuput Oil, Ferrosoferric Phosphate, Glycyrrhiza Glabra, Potassium Dichromate, Lachesis Muta Venom, Mentha Piperita, Mercury, Naja Naja Venom, Sodium Carbonate, Sodium Sulfate, Nitric Acid, Strychnos Nux-vomica Seed, Phosphorus, Phytolacca Americana Root, Pulsatilla Vulgaris, Spongia Officinalis Skeleton, Roasted, Tin, Lobaria Pulmonaria, Thuja Occidentalis Leafy Twig, Ulmus Rubra Bark, Verbascum Thapsus, Echinacea, Unspecified
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Throat Care  Formulated for symptoms associated with throat conditions such as dryness, irritation, inflammation, pain and hoarseness.

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 purfied water.  Sensitive persons begin with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Aconitum nap. 15x, Apis mel. 15x, Arum dracontium 15x, Belladonna 15x, Bryonia 15x, Cajuputum 15x, Ferrum phosphoricum 15x, Glycyrrhiza glabra 15x, Kali bic.15x, Lachesis 15x, Mentha piperita 15x, Merc. viv. 15x, Naja 15x, Nat. carb. 15x, Nat. sulphuricum 15x, Nitricum ac. 15x, Nux vom.15x, Phosphorus 15x, Phytolacca 15x, Pulsatilla 15x, Spongia 15x, Stannum met. 15x, Sticta 15x, Thuja occ. 15x, Ulmus fulva 15x, Verbascum 15x, Echinacea 3x.

OTC - PURPOSE SECTION

Formulated for symptoms associated with throat conditions such as dryness, irritation, inflammation, pain and hoarseness.

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55714-2249-02020-01-31C16284748780-19d75b9d0-2aa6-f424-e053-dadaa90a57ceThroat Care
55714-2249-12020-01-31C16284748780-19d75b9d0-2aa6-f424-e053-dadaa90a57ceThroat Care
55714-2249-22020-01-31C16284748780-19d75b9d0-2aa6-f424-e053-dadaa90a57ceThroat Care

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-2249-0Throat Care7.08 g in 1 BOTTLE, GLASSPELLET7.082
55714-2249-1Throat Care28.35 g in 1 BOTTLE, GLASSPELLET28.352
55714-2249-2Throat Care56.7 g in 1 BOTTLE, GLASSPELLET56.72

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-2249THROAT CARE (ACONITUM NAP., APIS MEL., ARUM DRACONTIUM, BELLADONNA, BRYONIA, CAJUPUTUM, FERRUM PHOSPHORICUM, GLYCYRRHIZA GLABRA, KALI BIC., LACHESIS, MENTHA PIPERITA, MERC. VIV., NAJA, NAT. CARB., NAT. SULPHURICUM, NITRICUM AC., NUX VOM., PHOSPHORUS, PHYTOLACCA, PULSATILLA, SPONGIA, STANNUM MET., STICTA, THUJA OCC., ULMUS FULVA, VERBASCUM, ECHINACEA) PELLET [NEWTON LABORATORIES, INC.]2Legacy NDC, 3 package rows20131015_4c3ed3ce-e70d-1fb1-bec6-da99f18506cb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aconitum NapellusACTIVE INGREDIENTU0NQ8555JD2
Apis MelliferaACTIVE INGREDIENT7S82P3R43Z2
Arisaema Dracontium RootACTIVE INGREDIENT73BHJ429FF2
Atropa BelladonnaACTIVE INGREDIENTWQZ3G9PF0H2
Bryonia Alba RootACTIVE INGREDIENTT7J046YI2B2
Cajuput OilACTIVE INGREDIENTJ3TO6BUQ372
Echinacea, UnspecifiedACTIVE INGREDIENT4N9P6CC1DX2
Ferrosoferric PhosphateACTIVE INGREDIENT91GQH8I5F72
Glycyrrhiza GlabraACTIVE INGREDIENT2788Z9758H2
Lachesis Muta VenomACTIVE INGREDIENTVSW71SS07I2
Lobaria PulmonariaACTIVE INGREDIENTD1YM0P5Z2T2
Mentha PiperitaACTIVE INGREDIENT79M2M2UDA92
MercuryACTIVE INGREDIENTFXS1BY2PGL2
Naja Naja VenomACTIVE INGREDIENTZZ4AG7L7VM2
Nitric AcidACTIVE INGREDIENT411VRN1TV42
PhosphorusACTIVE INGREDIENT27YLU75U4W2
Phytolacca Americana RootACTIVE INGREDIENT11E6VI8VEG2
Potassium DichromateACTIVE INGREDIENTT4423S18FM2
Pulsatilla VulgarisACTIVE INGREDIENTI76KB35JEV2
Sodium CarbonateACTIVE INGREDIENT45P3261C7T2
Sodium SulfateACTIVE INGREDIENT0YPR65R21J2
Spongia Officinalis Skeleton, RoastedACTIVE INGREDIENT1PIP394IID2
Strychnos Nux-vomica SeedACTIVE INGREDIENT269XH139192
Thuja Occidentalis Leafy TwigACTIVE INGREDIENT1NT28V93972
TinACTIVE INGREDIENT387GMG9FH52
Ulmus Rubra BarkACTIVE INGREDIENT91QY4PXU8Q2
Verbascum ThapsusACTIVE INGREDIENTC9TD27U1722
Aconitum NapellusACTIVE MOIETYU0NQ8555JD2
Apis MelliferaACTIVE MOIETY7S82P3R43Z2
Arisaema Dracontium RootACTIVE MOIETY73BHJ429FF2
Atropa BelladonnaACTIVE MOIETYWQZ3G9PF0H2
Bryonia Alba RootACTIVE MOIETYT7J046YI2B2
Cajuput OilACTIVE MOIETYJ3TO6BUQ372
Carbonate IonACTIVE MOIETY7UJQ5OPE7D2
Dichromate IonACTIVE MOIETY9LKY4BFN2V2
Echinacea, UnspecifiedACTIVE MOIETY4N9P6CC1DX2
Ferrosoferric PhosphateACTIVE MOIETY91GQH8I5F72
Glycyrrhiza GlabraACTIVE MOIETY2788Z9758H2
Lachesis Muta VenomACTIVE MOIETYVSW71SS07I2
Lobaria PulmonariaACTIVE MOIETYD1YM0P5Z2T2
Mentha PiperitaACTIVE MOIETY79M2M2UDA92
MercuryACTIVE MOIETYFXS1BY2PGL2
Naja Naja VenomACTIVE MOIETYZZ4AG7L7VM2
Nitric AcidACTIVE MOIETY411VRN1TV42
PhosphorusACTIVE MOIETY27YLU75U4W2
Phytolacca Americana RootACTIVE MOIETY11E6VI8VEG2
Pulsatilla VulgarisACTIVE MOIETYI76KB35JEV2
Sodium Sulfate AnhydrousACTIVE MOIETY36KCS0R7502
Spongia Officinalis Skeleton, RoastedACTIVE MOIETY1PIP394IID2
Strychnos Nux-vomica SeedACTIVE MOIETY269XH139192
Thuja Occidentalis Leafy TwigACTIVE MOIETY1NT28V93972
TinACTIVE MOIETY387GMG9FH52
Ulmus Rubra BarkACTIVE MOIETY91QY4PXU8Q2
Verbascum ThapsusACTIVE MOIETYC9TD27U1722
SucroseINACTIVE INGREDIENTC151H8M5542

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-224955714-2249-1, 55714-2249-2, 55714-2249-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
SucroseSUCROSEC151H8M554TABLET, DELAYED RELEASE / ORAL295.33 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE / ORAL3568 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS2000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / SUBCUTANEOUS47.75 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, CHEWABLE / ORAL7258 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION / INTRAVENOUS1950 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS308 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SOLUTION / ORAL42596 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, EXTENDED RELEASE / ORAL284.54 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / BUCCAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED, EXTENDED RELEASE / ORAL86 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CONCENTRATE / ORAL4800 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, EXTENDED RELEASE / ORAL619 mgExact 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
SucroseSUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554ELIXIR / ORAL18000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS1 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, FILM COATED / ORAL145 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTABLE, LIPOSOMAL / INTRAVENOUS7560 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / BUCCALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS900 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SOLUTION / RECTAL35.42 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554DROPS / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554PASTILLE / ORAL426 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, DELAYED RELEASE / ORAL955 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL18790 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554CAPSULE, COATED PELLETS / ORAL59.8 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554GRANULE, FOR SUSPENSION / ORAL31885 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554POWDER, FOR SOLUTION / ORAL38666 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554WAFER / ORAL155.2 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SOLUTION / INTRAVENOUSNAExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554SUSPENSION, EXTENDED RELEASE / ORAL5400 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET, COATED / ORAL516.42 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554LOZENGE / TRANSMUCOSAL1255 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / ORAL4249 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, EMULSION / INTRAVENOUS970 mgExact identifier — unii candidate
48 equally ranked IID candidates
SucroseSUCROSEC151H8M554TABLET / SUBLINGUAL109 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
4e6cf33f-eedd-b1b0-c10a-72035358ef284c3ed3ce-e70d-1fb1-bec6-da99f18506cb2011-03-01WarningsExact identifier
spl id: 4e6cf33f-eedd-b1b0-c10a-72035358ef28
spl set id: 4c3ed3ce-e70d-1fb1-bec6-da99f18506cb

Reported adverse events (FAERS/openFDA)#

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