LUMOe SKIN2 Skin Sensitivity

Manufacturer
Applied Bioenergetics, 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#

ProductLUMOe SKIN2 Skin Sensitivity
Active ingredientSPIGELIA ANTHELMIA, PHYTOLACCA AMERICANA ROOT, NERIUM OLEANDER LEAF, CLEMATIS RECTA FLOWERING TOP
Label structure11 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Spigelia anthelmia 12c
Phytolacca decandra 12c
Oleander 12c
Clematis erecta 12c

OTC - PURPOSE SECTION

Purpose*
Spigelia anthelmia  ............................................................ Painful sensitive skin
Phytolacca decandra  ................................................ Rash, erythema (redness)
Oleander  .................................................................. Very sensitive skin, itching
Clematis erecta  ....................................................................... Itchy painful skin

INDICATIONS & USAGE SECTION

Uses* Temporarily Relieves Minor and Occasional Symptoms:
• painful sensitive skin • rash • redness • itchy

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 3 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: At the onset of symptoms 3 tablets, every 30
minutes for 3 hours. Then 3 tablets every hour up to 6 times a day for 3 days until
symptoms are relieved 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.

LUMOe SKIN-2 Skin Sensitivity

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LUMOe

Homeopathy in a Whole New Light

SKIN-2
Skin Sensitivity*

180
Chewable Tablets
HOMEOPATHIC REMEDY

Distributed by Applied BioEnergetics LLC 9205 W Russell Rd Ste 240 Las Vegas, NV 89148

LUMO Skin2LUMO Skin2

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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
81425-008-10LUMOe SKIN2 Skin Sensitivity180 in 1 BOTTLETABLET, CHEWABLE1802

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81425-00881425-008-10

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
12024-10-01full-release2026-06-01 02:28:08

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
LUMOe SKIN2 Skin SensitivitySPIGELIA ANTHELMIA, PHYTOLACCA DECANDRA, OLEANDER, CLEMATIS ERECTAApplied Bioenergetics, LLC13a662fb-53b6-4449-99b7-2e50fef7a6a62025-11-10WarningsExact identifier
ndc (package): 81425-008-10
ndc (product): 81425-008
ndc11 (package): 81425000810
spl id: 63990c61-76eb-4696-9b52-e619db6c1c86
spl set id: 13a662fb-53b6-4449-99b7-2e50fef7a6a6

Reported adverse events (FAERS/openFDA)#

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