ABELMOSCHUS- abelmoschus moschatus seed 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 60512-6435-1

ACTIVE INGREDIENT HPUS

ABELMOSCHUS 6X

(Abelmoschus)

NIGHT FEARS

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

ABELMOSCHUS 
abelmoschus pellet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6435
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88) (ABELMOSCHUS MOSCHATUS SEED - UNII:UN2QZ55I88) ABELMOSCHUS MOSCHATUS SEED 6 [hp_X]
Inactive Ingredients
Ingredient Name Strength
LACTOSE (UNII: J2B2A4N98G)  
SUCROSE (UNII: C151H8M554)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60512-6435-1 80 in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 11/14/2013
Labeler - HOMEOLAB USA INC (202032533)
Registrant - HOMEOLAB USA INC. (202032533)
Establishment
Name Address ID/FEI Business Operations
HOMEOLAB USA INC 202032533 manufacture(60512-6435)

Revised: 11/2013
Document Id: 45084b0d-210b-4fc5-afa7-2f83fb28924e
Set id: 534ed9f1-2763-4fd5-8ba9-0cd7e1aa5e5d
Version: 1
Effective Time: 20131114
 
HOMEOLAB USA INC