LUMOe SKIN1 Skin Remedy
- 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 02:37:27
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients
Kali muriaticum 12c
Prunus spinosa 30c
Silicea 30c
Sarsaparilla 30c
OTC - PURPOSE SECTION
Purpose*
Kali muriaticum .......................................... Itchy, erythema (redness), blemish
Prunus spinosa ............................................................. Headaches, sacral pain
Silicea .................................................................................. Itchy sensitive skin
Sarsaparilla ...................................................................... Localized crusty skin
INDICATIONS & USAGE SECTION
Uses*Temporarily Relieves Minor and Occasional Symptoms:
• itchy • redness • blemish • headaches • sacral pain • sensitive crusty skin
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
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-1 Remedy* Localized Itchy, Irritated Skin* Labeling
LUMOe
Homeopathy in a Whole New Light
SKIN-1
Skin Remedy*
Localized Itchy,
Irritated Skin*
180
Chewable Tablets
HOMEOPATHIC REMEDY
Distributed by Applied BioEnergetics LLC 9205 W Russell Rd Ste 240 Las Vegas, NV 89148
res
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81425-007-10 | LUMOe SKIN1 Skin Remedy | 180 in 1 BOTTLE | TABLET, CHEWABLE | 180 | 2 |
Products#
Every source-derived product name is available through these pages.
- LUMOe SKIN1 Skin Remedy
- Kali muriaticum, Prunus spinosa, Silicea, Sarsaparilla
- POTASSIUM CHLORIDE
- POTASSIUM CATION
- PRUNUS SPINOSA FLOWER BUD
- SILICON DIOXIDE
- SMILAX ORNATA ROOT
- DEXTROSE
- MAGNESIUM STEARATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81425-007 | 81425-007-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM CHLORIDE | 660YQ98I10 | ACTIM |
| PRUNUS SPINOSA FLOWER BUD | 53Y84VPS2W | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| SMILAX ORNATA ROOT | 2H1576D5WG | ACTIB |
| DEXTROSE | IY9XDZ35W2 | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 1 | 2024-09-30 | full-release | 2026-06-01 02:28:12 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| LUMOe SKIN1 Skin Remedy | KALI MURIATICUM, PRUNUS SPINOSA, SILICEA, SARSAPARILLA | Applied Bioenergetics, LLC | d4d7fd2f-66bf-407d-ad36-2462e880b9f5 | 2025-11-10 | Warnings | 81425-007-10 81425-007 81425000710 507e1913-f6b0-4693-a99c-77d080e68294 d4d7fd2f-66bf-407d-ad36-2462e880b9f5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
