ACNE - kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar suphuris calcareum, tablet 
Apotheca Company

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.

----------

Acne Pill Russia

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


For treatment of the pimples and blemishes of Acne.


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

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

Keep out of the reach of children.

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.

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



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 INGREDIENTS:  Lactose, Magnesium stearate.


KEEP OUT OF REACH OF CHILDREN.


For treatment of the pimples and blemishes of Acne.


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


LOMA LUX

LOMA LUX ACNE PILL

Dermatologist Developed

For treatment of the pimples and blemishes of Acne

TAKE ORALLY

100 TABLETS

HOMEOPATHIC MEDICINE

Acne Pill Russia

ACNE 
kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar suphuris calcareum, tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-0710
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM BROMIDE (UNII: OSD78555ZM) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM BROMIDE1 [hp_X]
SODIUM BROMIDE (UNII: LC1V549NOM) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BROMIDE2 [hp_X]
NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68) (NICKEL - UNII:7OV03QG267) NICKEL SULFATE HEXAHYDRATE6 [hp_X]
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR6 [hp_X]
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFIDE9 [hp_X]
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
Colorwhite (off white) Scoreno score
ShapeROUND (cylindrical) Size9mm
FlavorImprint Code LL;
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57520-0710-31 in 1 CARTON
1NDC:57520-0710-21 in 1 CARTON
1NDC:57520-0710-1100 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/15/2011
Labeler - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture

Revised: 7/2011
Document Id: 51a649b9-ef27-4816-a50a-982233340909
Set id: b6c8565d-3e51-46bc-acb4-3365953ec5c8
Version: 1
Effective Time: 20110715
 
Apotheca Company