DIGITALIS PURPUREA- digitalis purpurea pellet 
HOMEOLAB USA INC.

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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HOMEOPATHIC MEDICINE NDC 60512-6643-1

ACTIVE INGREDIENT HPUS

DIGITALIS PURPUREA 8X

Digitalis

ANXIETY, FAINTNESS*

USE

For self-limiting condition listed above or as directed by a health professional.

WARNINGS

Do not use if pellet-dispenser seal is broken.

Stop use and ask a doctor if symptoms persist more than 3 days or worsen.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

DIRECTIONS

Adults: Allow 3 or 4 pellets to dissolve in the mouth 3 times a day until symptoms are relieved or as directed by a health professional.

OTHER INFORMATION

Store at room temperature.

INACTIVE INGREDIENTS

Lactose, sucrose.

The letters 'HPUS' indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

*These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

80 Pellets

Pellet dispenser

Mfd for: HOMEOLAB USA

3025 De L'Assomption, Montreal, QC, H1N 2H2, CANADA

1-800-404-4666 / www.homeolab.com

Product of Canada

LABEL

IMAGE OF TUBE LABEL

DIGITALIS PURPUREA 
digitalis purpurea pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60512-6643
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIGITALIS (UNII: F1T8QT9U8B) (DIGITALIS - UNII:F1T8QT9U8B) DIGITALIS8 [hp_X]
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60512-6643-180 in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic11/18/2013
Labeler - HOMEOLAB USA INC. (202032533)
Registrant - HOMEOLAB USA INC. (202032533)
Establishment
NameAddressID/FEIBusiness Operations
HOMEOLAB USA INC.202032533manufacture(60512-6643)

Revised: 11/2013
Document Id: b428c3f0-14c5-441d-a208-d39d3ad9e236
Set id: 60d720e1-1110-4f2b-85fe-2f5346e3a450
Version: 1
Effective Time: 20131118
 
HOMEOLAB USA INC.