PSORIASIS- niccolum sulphuricum, natrum bromatum, zincum bromatum, kali bromatum, kali sulphuricum. liquid

PSORIASIS by

Drug Labeling and Warnings

PSORIASIS by is a Homeopathic medication manufactured, distributed, or labeled by PLYMOUTH HEALTHCARE PRODUCTS LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

Uses: For temporary relief from scaling, flaking, redness & itching associated with Psoriasis, Seborrheic Dermatitis, Dandruff.

WARNINGS

Warnings:

• DO NOT USE * if you have kidney disease *in children under 12 years of age.
• Ask a doctor before use if you have a known sensitivity to any ingredient in LomaLux® Psoriasis ingredients, nickel or costume jewelry.
• When using this product use 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.

• Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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

Inactive Ingredients: Alcohol USP 2%, Methyl Paraben, Propyl Paraben, Purified Water.

QUESTIONS

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

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

Relieves

Itching

Redness

Scaling

Reduces

Inflammation

Irritation

Prevents

Recurrences

INGREDIENTS AND APPEARANCE

PSORIASIS 
niccolum sulphuricum, natrum bromatum, zincum bromatum, kali bromatum, kali sulphuricum. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61480-105
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM)	NICKEL SULFATE HEXAHYDRATE	3 [hp_X]  in 237 mL
SODIUM BROMIDE (UNII: LC1V549NOM) (BROMIDE ION - UNII:952902IX06)	SODIUM BROMIDE	2 [hp_X]  in 237 mL
ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37)	ZINC BROMIDE	4 [hp_X]  in 237 mL
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06)	POTASSIUM BROMIDE	1 [hp_X]  in 237 mL
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG)	POTASSIUM SULFATE	4 [hp_X]  in 237 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61480-105-03	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/12/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/12/2016

Labeler - PLYMOUTH HEALTHCARE PRODUCTS LLC (079330314)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(61480-105)