Label: AMBRA GRISEA- ambra grisea pellet
- NDC Code(s): 60512-7101-1
- Packager: HOMEOLAB USA INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Updated October 22, 2013
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- ACTIVE INGREDIENT HPUS
AMBRA GRISEA 2X
For self-limiting condition listed above or as directed by a health professional.Close
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.Close
- OTHER INFORMATION
Store at room temperature.Close
- INACTIVE INGREDIENTS
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.
Mfd for: HOMEOLAB USA INC., 3025 De L`Assomption, Montreal, QC, H1N 2H2, CANADA
Product of CanadaClose
- INGREDIENTS AND APPEARANCE
ambra grisea pellet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-7101 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C) AMBERGRIS 2 [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:60512-7101-1 80 in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/11/1995 Labeler - HOMEOLAB USA INC. (202032533) Registrant - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-7101)