FDA.reportPublic FDA data

Borago Lavender

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:30:08

Label at a glance#

ProductBorago Lavender
Active ingredientMELILOTUS INDICUS SEED, HORSE CHESTNUT, BORAGE
Label structure9 sections

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: 100 gm contains: 20 gm Aesculus (Horse chestnut seed) 1X, 20 gm Borago (Borage) 1X,
12 gm Melilotus (Yellow sweet clover) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Spring water, Organic cane alcohol, Witch Hazel distillate, Magnesium aluminum silicate,
Lavender oil, 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 LotionBorago Lavender Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2144-5Borago Lavender120 g in 1 TUBELOTION1205

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2144BORAGO LAVENDER LOTION [URIEL PHARMACY INC.]5Current NDC, Legacy NDC, 1 package rows20250109_d2b92916-4b04-ef41-e053-2995a90a8e0d.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-214448951-2144-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
XANTHAN GUMTTV12P4NEEIACT
MELILOTUS INDICUS SEEDF22I9R6Q0XACTIB
SORBIC ACIDX045WJ989BIACT
TEA TREE OILVIF565UC2GIACT
CITRUS PARADISI SEED12F08874Y7IACT
HORSE CHESTNUT3C18L6RJAZACTIB
ALCOHOL3K9958V90MIACT
BORAGEPB618V0K2WACTIB
WATER059QF0KO0RIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
LAVENDER OILZBP1YXW0H8IACT
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT

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
Borago LavenderBORAGO LAVENDERUriel Pharmacy Inc.d2b92916-4b04-ef41-e053-2995a90a8e0d2025-01-07WarningsExact identifier
ndc (package): 48951-2144-5
ndc (product): 48951-2144
ndc11 (package): 48951214405
spl id: 2b25361d-63b5-4e7f-e063-6394a90a935e
spl set id: d2b92916-4b04-ef41-e053-2995a90a8e0d

Reported adverse events (FAERS/openFDA)#

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