ACNE - kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar sulphurs 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.

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AcnePill

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 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.



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 THE 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 AcnePill

Dermatologist Developed

TAKE ORALLY

For treatment of the pimples and blemishes of Acne

100 TABLETS

HOMEOPATHIC MEDICINE

AcnePill

ACNE 
kali bromatum, natrum bromatum, niccolum sulphuricum, sulphur, hepar sulphurs calcareum, tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-0711
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:57520-0711-31 in 1 CARTON
1NDC:57520-0711-21 in 1 CARTON
1NDC:57520-0711-1100 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/29/2011
Labeler - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture

Revised: 6/2011
Document Id: eda9f5bc-1a20-4591-b1c1-3b015952c8db
Set id: f4ca87b4-e222-4c90-9423-c84b6a5668ad
Version: 1
Effective Time: 20110629
 
Apotheca Company