TOTAL MERCURY

Manufacturer
White Manufacturing Inc. DBA Micro-West
Effective date
2021-01-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:14:15

Label at a glance#

ProductTOTAL MERCURY
Active ingredientMERCURY
Label structure9 sections

Dosage and administration

DIRECTIONS: ORALLY 6 DROPS ORALLY, 4 TIMES A DAY.FOR AGES 2 TO ADULT

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

MERCURIUS VIVUS [HPUS]  12X,30X,200C,1M

Contains equal volumes of each ingredient.

PURPOSE

OTC - PURPOSE SECTION

FOR THE TEMPORARY RELIEF OF DIZZINESS, DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

INDICATIONS & USAGE SECTION

INDICATIONS :FOR THE TEMPORARY RELIEF OF DIZZINESS,FEELING  DISCOURAGED, DEPRESSION, PAINFUL DRYNESS OF THROAT

WARNING

WARNINGS SECTION

WARNING:STOP USE AND CALL A DOCTOR IF SYMPTOMS PERSIST OR WORSEN. IF PREGNANT ORBREAST-FEEDING CONSULT A HEALTHCARE PROFESSIONAL BEFORE USE.CONTAINS ALCOHOL, IN CASE OF ACCIDENTAL OVERDOSE, CONSULT A POISON CONTROL CENTER IMMEDIATELY

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: ORALLY 6 DROPS ORALLY, 4 TIMES A DAY.FOR AGES 2 TO ADULT

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

 ALCOHOL (20% V/V,PURIFIED WATER)

MANUFACTURE

SPL UNCLASSIFIED SECTION

MANUFACTURED FOR MICRO-WEST

DOUGLAS, WY 82633

1-307-358-5066

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61657-0961-1

MICRO-WEST

Homeopathic

4 Tier Multi-Potency

TOTAL MERCURY

Product #: 0961

1.0 fl oz bottle label1.0 fl oz bottle label

1.0 fl oz (29.6 mL)

Ethanol 20%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61657-0961-1TOTAL MERCURY30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61657-0961TOTAL MERCURY (MERCURIUS VIVUS) LIQUID [WHITE MANUFACTURING INC. DBA MICRO-WEST]5Current NDC, Legacy NDC, 1 package rows20210123_a8f0780c-70fa-4b88-ac46-e37e4ed37f97.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MERCURYACTIVE INGREDIENTFXS1BY2PGL2
MERCURYACTIVE MOIETYFXS1BY2PGL2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61657-096161657-0961-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
MERCURYFXS1BY2PGLACTIB

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
TOTAL MERCURYMERCURIUS VIVUSWhite Manufacturing Inc. DBA Micro-Westa8f0780c-70fa-4b88-ac46-e37e4ed37f972021-01-21WarningsExact identifier
ndc (package): 61657-0961-1
ndc (product): 61657-0961
ndc11 (package): 61657096101
spl id: b9703ce2-3dc1-11b5-e053-2a95a90aed81
spl set id: a8f0780c-70fa-4b88-ac46-e37e4ed37f97

Reported adverse events (FAERS/openFDA)#

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