LUMO Live Vitality Boost

Manufacturer
Applied Bioenergetics, LLC
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:37:27

Label at a glance#

ProductLUMO Live Vitality Boost
Active ingredientARNICA MONTANA, EUPHORBIA RESINIFERA RESIN, PULSATILLA PRATENSIS WHOLE, SOLANUM NIGRUM WHOLE
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Arnica montana 30c
Euphorbium officinarum 30c
Pulsatilla 30c
Solanum nigrum 9c

OTC - PURPOSE SECTION

Purpose*
Arnica montana  ................................................... Fatigue, aches & pains, stress
Euphorbium officinarum ..................................................................Chills, fever
Pulsatilla ................................................................................................... Colds
Solanum nigrum ..................................................................................Headache

INDICATIONS & USAGE SECTION

Uses* Temporarily Relieves Minor and Occasional:
• fatigue • aches & pains • stress • chills • fever • colds • headache

WARNINGS SECTION

Warnings
• Ask a doctor before use in children under 12 years of age.
• Stop use and ask a doctor if symptoms persist for more than 7 days or worsen.
• If pregnant or breastfeeding, consult your health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions
• For adults and children 12 and over: 2 tablets, 4 times a day or as recommended
by your healthcare professional.
• For children under 12: Ask a doctor.

OTHER SAFETY INFORMATION

Other Information Store at room temperature. No artificial colors or flavors.

INACTIVE INGREDIENT SECTION

Inactive Ingredients dextrose, magnesium stearate, silicon dioxide

OTC - QUESTIONS SECTION

Questions? 1-888-786-1707 • info@Lumo-e.com • www.Lumo-e.com

SPL UNCLASSIFIED SECTION

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED
MEDICAL EVIDENCE. NOT FDA EVALUATED.

Product Label for LUMO-e Live Vitality Boost

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LUMO-e
Homeopathy in a Whole New Light

Live Vitality Boost

Aches & Pains,
Stress, Fatigue*

180
Chewable Tablets

HOMEOPATHIC REMEDY

Safety Sealed. Do not use if marked inner seal is disturbed or missing.

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED
MEDICAL EVIDENCE. NOT FDA EVALUATED.

Distributed by Applied BioEnergetics LLC 205 W Russell Rd Las Vegas, NV 89148

Alive -002Alive -002

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81425-002-10LUMO Live Vitality Boost180 in 1 BOTTLETABLET, CHEWABLE1804

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81425-00281425-002-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32024-12-31full-release2026-06-01 02:29:55

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
LUMO Live Vitality BoostARNICA MONTANA, EUPHORBIUM OFFICINARUM, PULSATILLA, SOLANUM NIGRUMApplied Bioenergetics, LLCe623e53d-85ec-47fe-ad64-59cb4288b10b2025-11-10WarningsExact identifier
ndc (package): 81425-002-10
ndc (product): 81425-002
ndc11 (package): 81425000210
spl id: 8f4f612b-be78-4d5c-afdb-a289aeaa8ed0
spl set id: e623e53d-85ec-47fe-ad64-59cb4288b10b

Reported adverse events (FAERS/openFDA)#

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