- ACTIVE INGREDIENT:
- HOMEOPATHIC INDICATIONS:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- HOMEOPATHIC INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
OCTOPAMINE
octopamine (hydrochloride) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0975 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOPAMINE HYDROCHLORIDE (UNII: 37YAS5L9HQ) (OCTOPAMINE - UNII:14O50WS8JD) OCTOPAMINE HYDROCHLORIDE 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-0975-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/16/2017 03/16/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/16/2017 03/16/2022 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0975) , api manufacture(43742-0975) , label(43742-0975) , pack(43742-0975)