Equisetum Essence Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:36

Label at a glance#

ProductEquisetum Essence Special Order
Active ingredientEQUISETUM ARVENSE TOP
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

For compresses: Use 2 teaspoons per cup of lukewarm water. For full bath: Use 2-3 tablespoons.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Equisetum (Common horsetail) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, 20% Organic cane alcohol

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: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

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

EquisetumEssenceSOEquisetumEssenceSO

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4136-6Equisetum Essence Special Order125 mL in 1 BOTTLE, GLASSLIQUID1251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4136EQUISETUM ESSENCE SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 1 package rows20180505_6b66699b-e593-3265-e053-2a91aa0a9db3.zip

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
48951-413648951-4136-6

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
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
6b66699b-e594-3265-e053-2a91aa0a9db36b66699b-e593-3265-e053-2a91aa0a9db32018-05-04WarningsExact identifier
spl id: 6b66699b-e594-3265-e053-2a91aa0a9db3
spl set id: 6b66699b-e593-3265-e053-2a91aa0a9db3

Reported adverse events (FAERS/openFDA)#

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