Mercurius 10/20/30 Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2014-12-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:06:14

Label at a glance#

ProductMercurius 10/20/30 Special Order

Active ingredientMERCURY

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Mercurius 10X/20X/30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing consult a doctor before using. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRODUCT LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-7136-3	2020-01-31	C162847	48780-1	9d75b9d0-0e59-f424-e053-dadaa90a57ce	Mercurius 10/20/30 Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-7136-3	Mercurius 10/20/30 Special Order	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-7136	MERCURIUS 10/20/30 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20141204_e95cb934-24ff-415e-90a8-65ecb01a02e4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
MERCURY	ACTIVE INGREDIENT	FXS1BY2PGL	1
MERCURY	ACTIVE MOIETY	FXS1BY2PGL	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

Mercurius 10/20/30 Special Order
MERCURY
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-7136	48951-7136-3

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
Name	UNII	Kind
MERCURY	FXS1BY2PGL	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
78d8ccb3-cce6-4afd-8b8b-70ddc078b2ef			e95cb934-24ff-415e-90a8-65ecb01a02e4	2014-12-03	Warnings	Exact identifier spl id: 78d8ccb3-cce6-4afd-8b8b-70ddc078b2ef spl set id: e95cb934-24ff-415e-90a8-65ecb01a02e4

Reported adverse events (FAERS/openFDA)#

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