CETRARIA ISLANDICA- cetraria islandica 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.

----------

HOMEOPATHIC MEDICINE NDC 60512-6582-1

ACTIVE INGREDIENT HPUS

CETRARIA ISLANDICA 1X

(Iceland Moss)


COUGH WITH EXPECTORATION

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.

QUESTIONS?

1-800-404-4666

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 INC., 3025 De L`Assomption, Montreal, QC, H1N 2H2, CANADA

Product of Canada

LABEL

image of tube label

CETRARIA ISLANDICA 
cetraria islandica pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60512-6582
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA SUBSP. ISLANDICA - UNII:BJ7YPN79A1) CETRARIA ISLANDICA SUBSP. ISLANDICA1 [hp_X]
Inactive Ingredients
Ingredient NameStrength
LACTOSE (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60512-6582-180 in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic10/11/1995
Labeler - HOMEOLAB USA INC. (202032533)
Registrant - HOMEOLAB USA INC. (202032533)
Establishment
NameAddressID/FEIBusiness Operations
HOMEOLAB USA INC.202032533manufacture(60512-6582)

Revised: 11/2013
Document Id: fdcb1441-b829-4ddf-a5b9-1a51624261ae
Set id: 7b5b9c63-6af9-446e-9fc2-b726b9e352d0
Version: 1
Effective Time: 20131104
 
HOMEOLAB USA INC.