Label: ANXIETY HP (aconitum napellus, argentum nitricum, arsenicum album, calcarea carbonica, ignatia amara, kali carbonicum, lachesis mutus, natrum muriaticum, phosphorus, pulsatilla- pratensis, staphysagria, stramonium liquid
- NDC Code(s): 44911-0675-1
- 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 June 9, 2023
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ACTIVE INGREDIENTS:
(in each drop) Aconitum Napellus 30X 8.33%, Argentum Nitricum 30X 8.33%, Arsenicum Album 30X 8.33%, Calcarea Carbonica 30X 8.33%, Ignatia Amara 30X 8.33%, Kali Carbonicum 30X 8.33%, Lachesis Mutus 30X 8.33%, Natrum Muriaticum 30X 8.33%, Phosphorus 30X 8.33%, Pulsatilla 30X 8.33%, Staphysagria 30X 8.33%, Stramonium 30X 8.33%.
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PURPOSE:
Aconitum Napellus – agitation,** Argentum Nitricum - anticipation,** Arsenicum Album – fear of disease,** Calcarea Carbonica - overwhelm,** Ignatia Amara - tension,** Kali Carbonicum - worry,** Lachesis Mutus - suspicion,** Natrum Muriaticum - sleeplessness,** Phosphorus - anxiety,** Pulsatilla – forsaken feeling,** Staphysagria - guilt,** Stramonium - fright.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
- 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
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ANXIETY HP
aconitum napellus, argentum nitricum, arsenicum album, calcarea carbonica, ignatia amara, kali carbonicum, lachesis mutus, natrum muriaticum, phosphorus, pulsatilla (pratensis), staphysagria, stramonium liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0675 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS WHOLE 30 [hp_X] in 1 mL SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 30 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 30 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X] in 1 mL STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (STRYCHNOS IGNATII SEED - UNII:1NM3M2487K) STRYCHNOS IGNATII SEED 30 [hp_X] in 1 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 30 [hp_X] in 1 mL LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 30 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 30 [hp_X] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_X] in 1 mL PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE 30 [hp_X] in 1 mL DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED 30 [hp_X] in 1 mL DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM 30 [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:44911-0675-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 06/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/09/2023 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0675) , api manufacture(44911-0675) , label(44911-0675) , pack(44911-0675)
