Label: AMBRA GRISEA pellet
- 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
- OTHER INFORMATION
- INACTIVE INGREDIENTS
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)