Juglans 14 Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2014-12-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:06:17

Label at a glance#

ProductJuglans 14 Special Order

Active ingredientENGLISH WALNUT

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 Ingredient: Juglans regia e testa 14X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: 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 use. Do not use if safety seal is broken or missing.

REFRIGERATE AFTER OPENING. BEST WHEN USED WITHIN 90 DAYS OF OPENING.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care 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
48951-6064-3	2020-01-31	C162847	48780-1	9d75b9d0-3a9f-f424-e053-dadaa90a57ce	Juglans 14 Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-6064-3	Juglans 14 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
48951-6064	JUGLANS 14 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20141223_4513d525-0ae7-4809-9dfe-a37b7cbf4b58.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ENGLISH WALNUT	ACTIVE INGREDIENT	1V3SHR7QB7	1
ENGLISH WALNUT	ACTIVE MOIETY	1V3SHR7QB7	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.

Juglans 14 Special Order
ENGLISH WALNUT
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-6064	48951-6064-3

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
ENGLISH WALNUT	1V3SHR7QB7	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
da95bfe9-48ee-4b27-9bd3-2213c428cb49			4513d525-0ae7-4809-9dfe-a37b7cbf4b58	2014-12-22	Warnings	Exact identifier spl id: da95bfe9-48ee-4b27-9bd3-2213c428cb49 spl set id: 4513d525-0ae7-4809-9dfe-a37b7cbf4b58

Reported adverse events (FAERS/openFDA)#

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