Label: GASTROPANPAR (pancreas suis, stomach- suis, arsenicum album, graphites, lycopodium clavatum, nux vomica, phosphorus, syzygium jambolanum liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 44911-0073-1 - Packager: Energique, 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 February 18, 2020
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- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN:
- INDICATIONS:
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INGREDIENTS AND APPEARANCE
GASTROPANPAR
pancreas suis, stomach (suis), arsenicum album, graphites, lycopodium clavatum, nux vomica, phosphorus, syzygium jambolanum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0073 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SUS SCROFA PANCREAS (UNII: 9Y3J3362RY) (SUS SCROFA PANCREAS - UNII:9Y3J3362RY) SUS SCROFA PANCREAS 6 [hp_X] in 1 mL SUS SCROFA STOMACH (UNII: T0920P9Z9A) (SUS SCROFA STOMACH - UNII:T0920P9Z9A) SUS SCROFA STOMACH 6 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 12 [hp_X] in 1 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 12 [hp_X] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 12 [hp_X] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (SYZYGIUM CUMINI SEED - UNII:820LSF646I) SYZYGIUM CUMINI SEED 12 [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:44911-0073-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 03/25/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/25/2013 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0073) , api manufacture(44911-0073) , label(44911-0073) , pack(44911-0073)