LAURx IMMUNE SUPPORT

Manufacturer
Laurel Rose LLC
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:37:26

Label at a glance#

ProductLAURx IMMUNE SUPPORT
Active ingredientNERIUM OLEANDER LEAF
Label structure13 sections

Indications and uses

For the temporary relief of symptoms of fever, associated with flu-like symptoms. Supports a healthy immune response.

Dosage and administration

Directions Adults and children over the age of 12: Measure 1 ml of liquid into the dropper and dispense under tongue. Hold under tongue for 1-3 minutes before swallowing. Take 1 ml every 4-6 hours. Do not exceed 4 ml in 24 hours. Children under the age of 12: consult a physician.

Label contents#

Full prescribing information#

Active Ingredient (in each 1ml dose)

OTC - ACTIVE INGREDIENT SECTION

Oleander HPUS* 4X

The letters "HPUS" indicate that the component in the product is officially monographed in the Homeopathic Phormacopoeia of the United States.

Purpose

OTC - PURPOSE SECTION

Immune Support

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms of fever, associated with flu-like symptoms. Supports a healthy immune response.

Warning

WARNINGS SECTION

Warning

if you have ever had an allergic reaction to this product or any of its ingredients.

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding ask a health professional before use.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. In case of overdose, get medical help or contact poison control right away.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or new symptoms occur

Ask doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have been diagnosed with a heart arrhythmia are taking a cardiac glycoside.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children over the age of 12:

Measure 1 ml of liquid into the dropper and dispense under tongue. Hold under tongue for

1-3 minutes before swallowing. Take 1 ml every

4-6 hours. Do not exceed 4 ml in 24 hours.

Children under the age of 12: consult a physician.

Other Information

SPL UNCLASSIFIED SECTION

Store at room temperature. Do not use if tamper evident seal is missing or broken.

Questions or Comments

OTC - QUESTIONS SECTION

Questions or Comments

Info@mylaurelrose.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

CartonCarton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85230-100-01LAURx IMMUNE SUPPORT1 in 1 CARTONLIQUID12
85230-100-01LAURx IMMUNE SUPPORT60 mL in 1 BOTTLELIQUID602

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
85230-10085230-100-01

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
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
NERIUM OLEANDER LEAF7KV510R6H6ACTIB

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
LAURx IMMUNE SUPPORTOLEANDERLaurel Rose LLC426255dc-8a67-9aa1-e063-6394a90ae0a72025-11-10WarningsExact identifier
ndc (package): 85230-100-01
ndc (product): 85230-100
ndc11 (package): 85230010001
spl id: 4343549f-8872-0009-e063-6294a90a41b0
spl set id: 426255dc-8a67-9aa1-e063-6394a90ae0a7

Reported adverse events (FAERS/openFDA)#

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