Sucrose

Manufacturer: Uriel Pharmacy Inc
Effective date: 2010-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:02:11

Label at a glance#

ProductSucrose

Active ingredientSUCROSE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866 642-2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Uses: Use according to standard homeopathic indications.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Dissolve under the tongue 3-4 times daily. Age 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: ask a doctor.

OTC-Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Saccharum officinale (sucrose) 1X HPUS.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Do not use section

OTC - DO NOT USE SECTION

Warnings: Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask doctor section

OTC - ASK DOCTOR SECTION

Consult a doctor if symptoms persist, if you are diabetic or intolerant of sugar.

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or nursing, consult a doctor before use.

Questions section

OTC - QUESTIONS SECTION

Questions? Uriel Pharmacy

866 642-2858 East Troy, WI 53120

www.urielpharmacy.com

NDC 48951-9999-2

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sucrose

Homeopathic Pellets

net wt. 1 oz. (1350 pellets)

sucrose pellets bottle label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-9999-2	2020-01-31	C162847	48780-1	9d75b9d0-e03e-f424-e053-dadaa90a57ce	Sucrose Pellets - 1 oz.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-9999-2	Sucrose	1350 in 1 BOTTLE, GLASS	PELLET	1350		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-9999	SUCROSE PELLET [URIEL PHARMACY INC]	1	Legacy NDC, 1 package rows	20100203_fa4e4ce0-1039-11df-8a39-0800200c9a66.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
SUCROSE	ACTIVE INGREDIENT	C151H8M554	1
SUCROSE	ACTIVE MOIETY	C151H8M554	1

Products#

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

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

Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-9999	48951-9999-2

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	ACTIB

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
b5cb3250-1038-11df-8a39-0800200c9a66			fa4e4ce0-1039-11df-8a39-0800200c9a66	2010-02-02		Exact identifier spl id: b5cb3250-1038-11df-8a39-0800200c9a66 spl set id: fa4e4ce0-1039-11df-8a39-0800200c9a66

Reported adverse events (FAERS/openFDA)#

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