FDA.reportPublic FDA data

Mercurius solubilis

Manufacturer
Newton Laboratories, Inc.
Effective date
2023-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:20:52

Label at a glance#

ProductMercurius solubilis
Active ingredientMERCURIUS SOLUBILIS
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Law of similiars; Sensitive gums & teeth; Sore throat; Excessive saliva

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) as needed or as directed by a health professional.

OTC - ACTIVE INGREDIENT SECTION

Mercurius solubilis 12x

OTC - PURPOSE SECTION

Law of similars; Sensitive gums & teeth; Sore throat; Excessive saliva

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

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

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.

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.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-9022-6Mercurius solubilis3 L in 1 BOTTLE, PLASTICLIQUID31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-9022MERCURIUS SOLUBILIS LIQUID [NEWTON LABORATORIES, INC.]1Current NDC, 1 package rows20230412_f9131e4c-f1db-59df-e053-6394a90abf2d.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-902255714-9022-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
MERCURIUS SOLUBILIS324Y4038G2ACTIB

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mercurius solubilisMERCURIUS SOLUBILISNewton Laboratories, Inc.f9131e4c-f1db-59df-e053-6394a90abf2d2023-04-11WarningsExact identifier
ndc (package): 55714-9022-6
ndc (product): 55714-9022
ndc11 (package): 55714902206
spl id: f9135130-75ee-e44e-e053-6394a90a9d8e
spl set id: f9131e4c-f1db-59df-e053-6394a90abf2d

Reported adverse events (FAERS/openFDA)#

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