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#

ProductPSORIASIS
Active ingredientNICKEL SULFATE HEXAHYDRATE, SODIUM BROMIDE, ZINC BROMIDE, POTASSIUM BROMIDE, POTASSIUM SULFATE
Label structure10 sections

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

carton artworkcarton artwork8 oz bottle label8 oz bottle label

OTC - PURPOSE SECTION

Relieves

Itching

Redness

Scaling

Reduces

Inflammation

Irritation

Prevents

Recurrences

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130000000000000GTIN-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 table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
95250459-30e4-45c1-b08a-993044f49109Product name220250805
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61480-105-03PSORIASIS237 mL in 1 BOTTLELIQUID2376

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61480-10561480-105-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
PSORIASISNICCOLUM SULPHURICUM, NATRUM BROMATUM, ZINCUM BROMATUM, KALI BROMATUM, KALI SULPHURICUM.PLYMOUTH HEALTHCARE PRODUCTS LLC7ad9e8ac-c8a3-4cab-8ab2-15feaf4bd3dc2025-11-20WarningsExact identifier
ndc (package): 61480-105-03
ndc (product): 61480-105
ndc11 (package): 61480010503
spl id: 440c889d-1e86-767e-e063-6394a90abaa8
spl set id: 7ad9e8ac-c8a3-4cab-8ab2-15feaf4bd3dc

Reported adverse events (FAERS/openFDA)#

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