NDC | 66096-122-05 |
Set ID | 69eaabac-dca6-481c-b10e-bf8759a657f7 |
Category | HUMAN PRESCRIPTION DRUG LABEL |
Packager | OHM PHARMA INC. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
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ACTIVE INGREDIENT
ACTIVE INGREDIENTS (HPUS*): Equal amounts of: Adrenal Gland 10X, Adrenocorticotrophin 10X, Cerebrum 14X, Liver Gland 10X, Pituitarum Posterium Gland 10X, Placenta 8X, Thyroidinum 8X.
*The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OHM PITUITARUM COMPLEX
adrenal gland, adrenocorticotrophin, cerebrum, liver gland, pituitarum posterium gland, placenta, thyroidinum. liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66096-122 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE 10 [hp_X] in 59 mL CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA) CORTICOTROPIN 10 [hp_X] in 59 mL SUS SCROFA CEREBRUM (UNII: 4GB5DQR532) (SUS SCROFA CEREBRUM - UNII:4GB5DQR532) SUS SCROFA CEREBRUM 14 [hp_X] in 59 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 10 [hp_X] in 59 mL SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND, POSTERIOR - UNII:E8S87O660T) SUS SCROFA PITUITARY GLAND, POSTERIOR 10 [hp_X] in 59 mL SUS SCROFA PLACENTA (UNII: C8CV8867O8) (SUS SCROFA PLACENTA - UNII:C8CV8867O8) SUS SCROFA PLACENTA 8 [hp_X] in 59 mL THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (THYROID, UNSPECIFIED - UNII:0B4FDL9I6P) THYROID, UNSPECIFIED 8 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-122-05 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/10/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/10/2017 Labeler - OHM PHARMA INC. (030572478) Registrant - OHM PHARMA INC. (030572478) Establishment Name Address ID/FEI Business Operations OHM PHARMA INC. 030572478 manufacture(66096-122)