Label: ADRENAPAR- aralia quinquefolia, avena sativa, glandula suprarenalis suis, hypothalamus suis, arsenicum iodatum, calcarea carbonica, ignatia amara, lycopodium clavatum, natrum muriaticum, nux vomica, phosphoricum acidum, phosphorus, zincum metallicum liquid
- NDC Code(s): 44911-0678-1
- 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 July 20, 2023
If you are a consumer or patient please visit this version.
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ACTIVE INGREDIENTS:
(in each drop) Arsenicum Iodatum 12X 9.07%, Calcarea Carbonica 12X 9.07%, Glandula Suprarenalis Suis 8X 9.07%, Hypothalamus Suis 8X 9.07%, Ignatia Amara 12X 9.07%, Lycopodium Clavatum 12X 9.07%, Natrum Muriaticum 12X 9.07%, Nux Vomica 12X 9.07%, Phosphorus 12X 9.07%, Phosphoricum Acidum 12X 9.07%, Zincum Metallicum 12X 9.07%, Aralia Quinquefolia 3X 0.10%, Avena Sativa 3X 0.10%.
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PURPOSES:
Arsenicum Iodatum – swelling**, Calcarea Carbonica – fatigue**, Glandula Suprarenalis Suis – apathy**, Hypothalamus Suis – sadness**, Ignatia Amara – low appetite**, Lycopodium Clavatum – faintness**, Natrum Muriaticum – heat intolerance**, Nux Vomica – early waking**, Phosphorus – thirst**, Phosphoricum Acidum – disinterest**, Zincum Metallicum – restlessness**, Aralia Quinquefolia – drowsiness**, Avena Sativa – sleeplessness**.
- USES:
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WARNINGS:
Stop use and ask a doctor if symptoms persist for more than 7 days.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING
Store in a cool, dry place.
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ADRENAPAR
aralia quinquefolia, avena sativa, glandula suprarenalis suis, hypothalamus suis, arsenicum iodatum, calcarea carbonica, ignatia amara, lycopodium clavatum, natrum muriaticum, nux vomica, phosphoricum acidum, phosphorus, zincum metallicum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0678 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMERICAN GINSENG (UNII: 8W75VCV53Q) (AMERICAN GINSENG - UNII:8W75VCV53Q) AMERICAN GINSENG 3 [hp_X] in 1 mL AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F) AVENA SATIVA FLOWERING TOP 3 [hp_X] in 1 mL SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND 8 [hp_X] in 1 mL SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (SUS SCROFA HYPOTHALAMUS - UNII:N6R0856Z79) SUS SCROFA HYPOTHALAMUS 8 [hp_X] in 1 mL ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIIODIDE 12 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X] in 1 mL STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED 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 SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 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 PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 12 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X] in 1 mL ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS) ZINC 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:44911-0678-1 60 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 07/20/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/20/2023 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0678) , api manufacture(44911-0678) , label(44911-0678) , pack(44911-0678)
