EUCALYPTUS GLOBULUS- eucalyptus globulus pellet

United States - English - NLM (National Library of Medicine)

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Active ingredient:
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6)
Available from:
HOMEOLAB USA INC.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
COLD AND FLU-LIKE SYMPTOMS* For self-limiting condition listed above or as directed by a health professional.
Authorization status:
unapproved homeopathic
Authorization number:
60512-6669-1

EUCALYPTUS GLOBULUS- eucalyptus globulus 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 60512-6669-1

ACTIVE INGREDIENT HPUS

EUCALYPTUS GLOBULUS 1X

Eucalyptus

COLD AND FLU-LIKE SYMPTOMS*

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

EUCALYPTUS GLOBULUS

eucalyptus globulus pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 0 512-6 6 6 9

Route of Administration

ORAL

HOMEOLAB USA INC.

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

EUCALYPTUS GLO BULUS LEAF (UNII: S546 YLW6 E6 ) (EUCALYPTUS GLOBULUS LEAF

- UNII:S546 YLW6 E6 )

EUCALYPTUS GLOBULUS

LEAF

1 [hp_X]

Inactive Ingredients

Ingredient Name

Stre ng th

LACTO SE (UNII: J2B2A4N9 8 G)

SUCRO SE (UNII: C151H8 M554)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 0 512-6 6 6 9 -1

8 0 in 1 TUBE

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

11/18 /20 13

Labeler -

HOMEOLAB USA INC. (202032533)

Registrant -

HOMEOLAB USA INC. (202032533)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

HOMEOLAB USA INC.

20 20 32533

ma nufa c ture (6 0 512-6 6 6 9 )

Revised: 11/2013

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