Borago Lavender cum Cupro

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2024-09-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:27:53

Label at a glance#

ProductBorago Lavender cum Cupro

Active ingredientMELILOTUS INDICUS SEED, CUPRIC SULFATE, BORAGE, HORSE CHESTNUT

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100gm contains: 20gm Aesculus (Horse chestnut seed) 1X, 20gm Borago (Borage) 1X, 13gm Melilotus (Yellow sweet clover) 1X, 40gm Cuprum sulfuricum (Copper sulfate) 2X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Spring water, Organic cane alcohol, Witch hazel extract, Magnesium aluminum silicate, Lavender oil, Silica gel, Xanthan gum, Sorbic acid, Tea tree oil,Grapefruit seed extract

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporarily relieves symptoms of varicose veins and leg cramps.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings:
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.

SHAKE WELL BEFORE USE.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Borago Lavender cum Cupro Lotion

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0306390c-dd77-4363-afe0-63c58088b2a1	Product name	1	20220120
503ea967-4b9c-48cf-9e87-c7975295849d	Product name	2	20220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-2153-8	2026-01-29	C162847	48780-1	49896155-aa7d-586f-e063-e6dba90add90	Borago Lavender cum Cupro

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-2153-8	Borago Lavender cum Cupro	120 g in 1 TUBE	LOTION	120		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-2153	BORAGO LAVENDER CUM CUPRO LOTION [URIEL PHARMACY, INC.]	1	1 package rows	20240907_21785860-6205-7875-e063-6294a90aa606.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Borago Lavender cum Cupro
MELILOTUS INDICUS SEED
LAVENDER OIL
TEA TREE OIL
CUPRIC SULFATE
CUPRIC CATION
XANTHAN GUM
BORAGE
HAMAMELIS VIRGINIANA TOP WATER
WATER
MAGNESIUM ALUMINUM SILICATE
SILICON DIOXIDE
SORBIC ACID
HORSE CHESTNUT
CITRUS PARADISI SEED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-2153	48951-2153-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MELILOTUS INDICUS SEED	F22I9R6Q0X	ACTIB
LAVENDER OIL	ZBP1YXW0H8	IACT
TEA TREE OIL	VIF565UC2G	IACT
CUPRIC SULFATE	LRX7AJ16DT	ACTIM
XANTHAN GUM	TTV12P4NEE	IACT
BORAGE	PB618V0K2W	ACTIB
HAMAMELIS VIRGINIANA TOP WATER	NT00Y05A2V	IACT
WATER	059QF0KO0R	IACT
MAGNESIUM ALUMINUM SILICATE	6M3P64V0NC	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
SORBIC ACID	X045WJ989B	IACT
HORSE CHESTNUT	3C18L6RJAZ	ACTIB
CITRUS PARADISI SEED	12F08874Y7	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
21784154-a791-7a18-e063-6294a90ab812			21785860-6205-7875-e063-6294a90aa606	2024-09-05	Warnings	Exact identifier spl id: 21784154-a791-7a18-e063-6294a90ab812 spl set id: 21785860-6205-7875-e063-6294a90aa606

Reported adverse events (FAERS/openFDA)#

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