PSORIASIS
- Manufacturer
- PLYMOUTH HEALTHCARE PRODUCTS LLC
- Effective date
- 2025-11-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-06-01 02:35:18
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Drug Facts
| Active Ingredients (in each teaspoon): | Purpose* |
| Niccolum Sulphuricum 3x (59.9%) | Skin Itching |
| Natrum Bromatum 2x (30%) | Calming Effect |
| Zincum Bromatum 4x (4%) | Skin Itching, Psoriasis Eruptions |
| Kali Bromatum 1x (3.5%) | Itching, Scaling & Redness |
| Kali Sulphuricum 4x (0.025%) | Scaling, Psoriasis Treatment |
INDICATIONS & USAGE SECTION
Uses: For temporary relief from scaling, flaking, redness & itching associated with Psoriasis, Seborrheic Dermatitis, Dandruff.
WARNINGS SECTION
Warnings:
- DO NOT USE* if you have kidney disease *in children under 12 years of age.
- Ask a doctor before use ifyou have a known sensitivity to any ingredient in LomaLux® Psoriasis ingredients, nickel or costume jewelry.
- When using this productuse only as directed.
- Stop use and ask a doctor if*symptoms do not improve, recur, are unusual *skin rash appears
- If pregnant or breast-feeding,ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions:Adults & Children 12 & Older: Take once per day as indicated on the chart below according to your weight:
WEIGHT DAILY DOSAGE BOTTLE LASTS
50 - 100 lbs. 1/2 Teaspoon 96 Days
100 - 150 lbs. 1 Teaspoon 48 Days
150 - 200 lbs. 1 1/2 Teaspoons 32 Days
Over 200 lbs. 2 Teaspoons 24 Days
For Optimal Absorption, take orally at Bedtime or in the Morning on an empty stomach. Do not eat or drink anything but water for 1 hour after taking. Increase dosage by 50% if symptoms do not improve after 4-5 months.
Recommended treatment course 4-5 months.
OTHER SAFETY INFORMATION
Other Information: DO NOT USE*if imprinted tamper evident band is broken or missing. *Store at room temperature, 68 to 77 Fahrenheit. Protect from light.
INACTIVE INGREDIENT SECTION
Inactive Ingredients:Alcohol USP 2%, Methyl Paraben, Propyl Paraben, Purified Water.
OTC - QUESTIONS SECTION
Questions? Comments? Side Effects?
Call 800-316-9636 or visit
www.lomalux.com
OTHER SAFETY INFORMATION
*These statements are based upon traditional homeopathic practice. They have not been evaluated by the Food & Drug Administration.
Distributed by Loma Lux Laboratories
6521 Davis Industrial Parkway, Solon, Ohio 44139 USA
SPL UNCLASSIFIED SECTION
Loma Lux founder, Dr. Steven A. Smith M.D. developed Loma Lux® Psoriasis as a natural treatment for his psoriasis patients. Extensive scientific research & rigorous testing led to this exclusive formulation that has helped psoriasis sufferers for decates.
Unlike many conventional creams and lotions which only treat the surface of the skin, LomaLux Psoriasis is taken internally to help attack psoriasis at its source, by helping to gently stimulate your body's own recovery response. To achieve maximum benefits & relief, a 4-5 month treatment plan is recommended.
Over a Decade of Safe, Effective Use with NO Known Side Effects.
Finally, Healthy Skin!
Countless Studies have documented the skin healing powers of minerals, including the world renowned Dead Sea for soothing relief of many skin conditions. LomaLux® Psoriasis contains many of the same minerals as found in the Dead Sea - for natural health & well-being. Join the thousands of LomaLux® Psoriasis users, who for decades have found natural relief.
5 POWERFUL ACTIVE INGREDIENTS to help fight Psoriasis & Seborrhea
In a Clinical Test: 85% of Psoriasis Patients Experienced Real Relief.
- Itching
- Redness
- Scaling
- Inflammation
- Irritation
CLINICAL STUDY DATA available at
www.lomalux.com
U.S. Patents No.5,171,581;5,681,593;5,433,954
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NEW ITEM
NDC#61480-105-03
NATURE CREATED. DERMATOLOGIST PERFECTED.™
LOMALUX® LABORATORIES
PSORIASIS
PATENTED MINERAL TECHNOLOGY
CLINICALLY PROVEN
Relieves
Itching
Redness
Scaling
Reduces
Inflammation
Irritation
Prevents
Recurrences
24 HOUR ONE DOSE
2% Alcohol
8 FL. OZ. (237 mL)
HOMEOPATHIC ORAL MEDICATION
OTC - PURPOSE SECTION
Relieves
Itching
Redness
Scaling
Reduces
Inflammation
Irritation
Prevents
Recurrences
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0000000000000 | GTIN-13: 0000000000000 EAN-13: 0000000000000 GTIN-12: 000000000000 UPC-A: 000000000000 GTIN storage (14 digits): 00000000000000 | Psoriasis - carton artwork.jpg, Psoriasis - 8 fl oz bottle label.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 95250459-30e4-45c1-b08a-993044f49109 | Product name | 2 | 20250805 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 26acd337-b838-40ac-bcbc-05c3b81c8712 | Product name | 1 | 20170323 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61480-105-03 | PSORIASIS | 237 mL in 1 BOTTLE | LIQUID | 237 | 6 |
Products#
Every source-derived product name is available through these pages.
- PSORIASIS
- Niccolum Sulphuricum, Natrum Bromatum, Zincum Bromatum, Kali Bromatum, Kali Sulphuricum.
- METHYLPARABEN
- PROPYLPARABEN
- WATER
- NICKEL SULFATE HEXAHYDRATE
- NICKEL CATION
- SODIUM BROMIDE
- BROMIDE ION
- ZINC BROMIDE
- ZINC CATION
- POTASSIUM BROMIDE
- POTASSIUM SULFATE
- SULFATE ION
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 61480-105 | 61480-105-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| METHYLPARABEN | A2I8C7HI9T | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| WATER | 059QF0KO0R | IACT |
| NICKEL SULFATE HEXAHYDRATE | JC9WZ4FK68 | ACTIB |
| SODIUM BROMIDE | LC1V549NOM | ACTIB |
| ZINC BROMIDE | OO7ZBU9703 | ACTIB |
| POTASSIUM BROMIDE | OSD78555ZM | ACTIB |
| POTASSIUM SULFATE | 1K573LC5TV | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| PSORIASIS | NICCOLUM SULPHURICUM, NATRUM BROMATUM, ZINCUM BROMATUM, KALI BROMATUM, KALI SULPHURICUM. | PLYMOUTH HEALTHCARE PRODUCTS LLC | 7ad9e8ac-c8a3-4cab-8ab2-15feaf4bd3dc | 2025-11-20 | Warnings | 61480-105-03 61480-105 61480010503 440c889d-1e86-767e-e063-6394a90abaa8 7ad9e8ac-c8a3-4cab-8ab2-15feaf4bd3dc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

