DANDRUFF- kali bromatum, kali muriaticum, kali sulphuricum, natrum muriaticum, sulphur, calcarea carbonica, niccolum sulphuricum. tablet

DANDRUFF by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENTS / PURPOSE

• Active ingredients (HPUS*) in each 750mg Pill: Purpose**
• Kali Bromatum 1X HPUS: Itching, Scaling & Redness
• Kali Muriaticum 1X HPUS: Dry, White Scales
• Kali Sulphuricum 1X HPUS: Flaking
• Natrum Muriaticum 1X HPUS: Oily Scalp, Itchy, Burning Scalp
• Sulphur 1X HPUS: Dry, Scaly, Itchy Skin & Scalp
• Calcarea Carbonica 3X HPUS: White, Crusty Scales
• Niccolum Sulphuricum 3X HPUS: Skin Itching

USES

Uses: For the temporary relief of Dandruff symptoms.** The claims for this product are based upon traditional homeopathic practice. They have not been reviewed by the FDA.

WARNINGS

Warnings:

 DO NOT USE

• if you have kidney disease
• in children under 12 years old
• children under 50 lbs
• if pregnant

Ask a doctor before use if

• you have a known sensitivity to nickel or costume jewelry
• a known sensitivity to any ingredients in this product

Stop use and ask a doctor if

• skin rash appears
• feelings of nervousness occur
• if condition worsens or does not improve after regular use of this product

 If pregnant, do not use.

If breast-feeding, ask a doctor before use.

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

Keep out of reach of children.

DIRECTIONS

Directions: Adults & Children 50 lbs & Up:

Take ONCE per day as indicated on the chart below according to your weight:

Weight Daily Dosage

50 - 100 lbs ...................... (2) Pills Daily

100 - 150 lbs .................... (4) Pills Daily

150 - 200 lbs .................... (6) Pills Daily

200 - 250 lbs .................... (8) Pills Daily

Over 250 lbs ..................... (10) Pills Daily

Swallow whole. 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.

OTHER INFORMATION

Other information:TAMPER EVIDENT - for your protection, this bottle has an imprinted seal around the neck. DO NOT USE if imprinted tamper evident seal band is broken or missing.

INACTIVE INGREDIENT

Inactive ingredients: Fumaric Acid, Magnesium Stearate, Maltodextrin, Microcrystalline Cellulose, Natural Blueberry Flavor, Organic Spirulina Powder, Sucrose.

QUESTIONS or COMMENTS?

Questions or Comments?

Call 800-316-9636, Monday through Friday, 9am-5pm EST or visit www.lomalux.com

Distributed by Loma Lux Laboratories: 6521 Davis Industrial Parkway, Solon, OH 44139 USA

OTHER SAFETY INFORMATION

WE TARGET DANDRUFF AT ITS SOURCE - FOR HEALTHY SCALP FROM WITHIN

Dandruff Pill works from the inside out to provide scalp relief from within. Just like your daily vitamin, Dandruff Pill is taken orally. With just one daily dose, Dandruff Pill's active mineral ingredients help relieve Dandruff symptoms.

NATURE CREATED - DERMATOLOGIST PERFECTED

We use only the finest quality ingredients in our exclusive formulation developed by our dermatologist founder to promote scalp health from within. A perfect blend of science and nature.

MADE IN THE USA

NATURAL active ingredients

LACTOSE FREE

VEGAN

GLUTEN FREE

EXCLUSIVE MINERAL TECHNOLOGY PROMOTES SCALP HEALTH

7 Active Mineral Ingredients help relieve dandruff symptoms of flaking, itchy scalp, dryness, and irritation. These unique inorganic minerals are all natural, earth derived.

WHEN USED REGULARLY, MAY HELP RELIEVE SYMPTOMS OF DANDRUFF

DERMATOLOGISTS DEVELOPED, FOR HEALTHY SKIN FROM WITHIN

UNIQUE! - CUSTOMED DOSAGE ACCORDING TO YOUR WEIGHT FOR OPTIMAL RESULTS

A 12 WEEK USE COURSE IS RECOMMENDED. CONTINUE TAKING AS LONG AS BENEFICIAL.

PRINCIPAL DISPLAY PANEL

NDC# 61480-310-01

LOMALUX LABORATORIES

DANDRUFF PILL™

HEALTHY SCALP FROM WITHIN™

Relieves Symptoms of Dandruff:

Itchy Scalp

Dryness/Irritation

Flaking

Oily Scalp

Promotes Scalp Health

HOMEOPATHIC ORAL MEDICATION

DERMATOLOGIST DEVELOPED

1 DAILY DOSE

144 PILLS

Relieves Symptoms of Dandruff:

Itchy Scalp

Dryness/Irritation

Flaking

Oily Scalp

Promotes Scalp Health

INGREDIENTS AND APPEARANCE

DANDRUFF 
kali bromatum, kali muriaticum, kali sulphuricum, natrum muriaticum, sulphur, calcarea carbonica, niccolum sulphuricum. tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61480-310
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06)	POTASSIUM BROMIDE	1 [hp_X]
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	1 [hp_X]
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG)	POTASSIUM SULFATE	1 [hp_X]
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	1 [hp_X]
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	1 [hp_X]
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	3 [hp_X]
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL CATION - UNII:OIS2CXW7AM)	NICKEL SULFATE HEXAHYDRATE	3 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
FUMARIC ACID (UNII: 88XHZ13131)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
BLUEBERRY (UNII: 253RUG1X1A)
SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white (off-white with speckles)	Score	2 pieces
Shape	ROUND	Size	11mm
Flavor	BLUEBERRY	Imprint Code	LL
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61480-310-01	144 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/24/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/24/2017

Labeler - PLYMOUTH HEALTHCARE PRODUCTS LLC (079330314)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(61480-310)