Label: 5 CHRONIC STRESS- aralia quinquefolia, fucus vesiculosus, solidago virgaurea, taraxacum officinale, trifolium pratense, hydrastis canadensis, arsenicum album, calcarea carbonica, carbo vegetabilis, ceanothus americanus, cyclamen europaeum, hepar sulphuris calcareum, natrum muriaticum, nux vomica, petroleum, phosphorus liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 55146-005-01 - Packager: Biotics Research Corporation
- 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 May 19, 2020
If you are a consumer or patient please visit this version.
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ACTIVE INGREDIENTS:
Aralia Quinquefolia 3X, 30C, Fucus Vesiculosus 3X, 30C, Solidago Virgaurea 3X, 30C, Taraxacum Officinale 3X, 30C, Trifolium Pratense 3X, 30C, Hydrastis Canadensis 5X, 30C, Arsenicum Album 30C, Calcarea Carbonica 30C, Carbo Vegetabilis 30C, Ceanothus Americanus 30C, Cyclamen Europaeum 30C, Hepar Sulphuris Calcareum 30C, Natrum Muriaticum 30C, Nux Vomica 30C, Petroleum30C, Phosphorus 30C.
- INDICATIONS:
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WARNINGS:
If symptoms persist or worsen, seek the advice of a healthcare professional.
Caution: Not recommended for pregnant or lactating women.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Tamper Seal: Sealed with an imprinted safety seal for your protection. Do not use if seal is missing or broken.
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INDICATIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
5 CHRONIC STRESS
aralia quinquefolia, fucus vesiculosus, solidago virgaurea, taraxacum officinale, trifolium pratense, hydrastis canadensis, arsenicum album, calcarea carbonica, carbo vegetabilis, ceanothus americanus, cyclamen europaeum, hepar sulphuris calcareum, natrum muriaticum, nux vomica, petroleum, phosphorus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55146-005 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 FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X] in 1 mL SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (SOLIDAGO VIRGAUREA FLOWERING TOP - UNII:5405K23S50) SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X] in 1 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 3 [hp_X] in 1 mL TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (TRIFOLIUM PRATENSE FLOWER - UNII:4JS0838828) TRIFOLIUM PRATENSE FLOWER 3 [hp_X] in 1 mL GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 5 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 30 [hp_C] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C] in 1 mL ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL 30 [hp_C] in 1 mL CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N) (CEANOTHUS AMERICANUS LEAF - UNII:25B1Y14T8N) CEANOTHUS AMERICANUS LEAF 30 [hp_C] in 1 mL CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (CYCLAMEN PURPURASCENS TUBER - UNII:G728143D8Q) CYCLAMEN PURPURASCENS TUBER 30 [hp_C] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 30 [hp_C] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 30 [hp_C] in 1 mL KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 30 [hp_C] in 1 mL PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 30 [hp_C] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SODIUM BENZOATE (UNII: OJ245FE5EU) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55146-005-01 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/11/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/11/2019 Labeler - Biotics Research Corporation (092487347) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(55146-005) , api manufacture(55146-005) , label(55146-005) , pack(55146-005)
