PSORIASIS- niccolum sulphuricum, natrum bromatum, zincum bromatum, kali bromatum, kali sulphuricum. liquid 
PLYMOUTH HEALTHCARE PRODUCTS LLC

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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LOMA LUX PSORIASIS

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 

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

Warnings:

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

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

Questions? Comments? Side Effects?

Call 800-316-9636 or visit www.lomalux.com

*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

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.

CLINICAL STUDY DATA available at www.lomalux.com

U.S. Patents No.5,171,581;5,681,593;5,433,954

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 artwork8 oz bottle label

Relieves

Itching

Redness

Scaling

Reduces

Inflammation

Irritation

Prevents

Recurrences

PSORIASIS 
niccolum sulphuricum, natrum bromatum, zincum bromatum, kali bromatum, kali sulphuricum. liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61480-105
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM) NICKEL SULFATE HEXAHYDRATE3 [hp_X]  in 237 mL
SODIUM BROMIDE (UNII: LC1V549NOM) (BROMIDE ION - UNII:952902IX06) SODIUM BROMIDE2 [hp_X]  in 237 mL
ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37) ZINC BROMIDE4 [hp_X]  in 237 mL
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06) POTASSIUM BROMIDE1 [hp_X]  in 237 mL
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG) POTASSIUM SULFATE4 [hp_X]  in 237 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61480-105-03237 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic12/12/2016
Labeler - PLYMOUTH HEALTHCARE PRODUCTS LLC (079330314)

Revised: 12/2021
Document Id: d44a6335-b07b-6659-e053-2995a90a1eee
Set id: 7ad9e8ac-c8a3-4cab-8ab2-15feaf4bd3dc
Version: 4
Effective Time: 20211229
 
PLYMOUTH HEALTHCARE PRODUCTS LLC