Label: AMMONIUM PHOSPHORICUM pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 60512-6173-1 - 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.
Drug Label Information
Updated October 22, 2013
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- ACTIVE INGREDIENT HPUS
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- INACTIVE INGREDIENTS
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INGREDIENTS AND APPEARANCE
AMMONIUM PHOSPHORICUM
ammonium phosphoricum pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6173 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) PHOSPHATE ION 3 [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:60512-6173-1 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(60512-6173)