ACNE- kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar sulphurs calcareum, tablet

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:  Kali bromatum 1X, Natrum bromatum 2X, Niccolum sulphuricum 6X, Sulphur 6X, Hepar sulphuris calcareum 9X.

PURPOSE

For treatment of the pimples and blemishes of acne.

WARNINGS

WARNINGS:  If symptoms persist or worsen, contact a physician. 

If pregnant or nursing, use only under the advice and supervision of a physician.

Keep our of the reach of children.

Safety Sealed for your protection.  Do not use if imprinted seal around bottle neck and cap is missing or broken.

CAUTION:  Use only as directed.

Do not give to children under six years old or use in the presence of kidney disease. 

If skin rash appears, or if nervous symptoms persist, recur frequently, or are unusual, discontinue use and consult a physician.

DOSAGE & ADMINISTRATION

DIRECTIONS:  Take once per day as indicated on chart below.  Continue use as long as it is beneficial to your overall condition.

WEIGHT            DAILY DOSAGE

50-100 lbs            One tablet

100-150 lbs          Two tablets

150-200 lbs          Three tablets

Over 200 lbs        Four tablets

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:  Lactose, Magnesium stearate.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF THE REACH OF CHILDREN.

INDICATIONS & USAGE

For treatment of the pimples and blemishes of Acne.

QUESTIONS

Manufactured for and dist. by:

LOMA LUX LABORATORIES

P.O. Box 702418

Tulsa, OK 74170-2418

Questions?  Call us:

1-866-LOMALUX

More information?  Visit our Web Site

AcnePill.com

PRINCIPAL DISPLAY PANEL

LOMA LUX

LOMA LUX AcnePill

Dermatologist Developed

TAKE ORALLY

For treatment of the pimples and blemishes of Acne

100 TABLETS

HOMEOPATHIC MEDICINE

INGREDIENTS AND APPEARANCE

ACNE 
kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar sulphurs calcareum, tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57520-0711
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM BROMIDE (UNII: OSD78555ZM) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM BROMIDE	1 [hp_X]
SODIUM BROMIDE (UNII: LC1V549NOM) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM BROMIDE	2 [hp_X]
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL - UNII:7OV03QG267)	NICKEL SULFATE HEXAHYDRATE	6 [hp_X]
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_X]
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFIDE	9 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white (off white)	Score	no score
Shape	ROUND (cylindrical)	Size	9mm
Flavor		Imprint Code	LL;
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57520-0711-3	1 in 1 CARTON
1	NDC: 57520-0711-2	1 in 1 CARTON
1	NDC: 57520-0711-1	100 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/29/2011

Labeler - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture