Label: EMF PROTECT AND BALANCE- alfalfa, fucus vesiculosus, kali phosphoricum, symphytum officinale, calcarea carbonica, ferrum metallicum, cadmium sulphuratum, hypericum perforatum, magnesia phosphorica, manganum metallicum, mercurius vivus, plumbum metallicum, ytterbium oxide, tarentula cubensis, x-ray, cuprum metallicum, silicea liquid
- NDC Code(s): 43742-1594-1
- Packager: Deseret Biologicals, Inc.
- Category: HUMAN OTC DRUG LABEL
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 9, 2024
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ACTIVE INGREDIENTS:
Alfalfa 3X, Cadmium Sulphuratum 12X, Calcarea Carbonica 8X, Cuprum Metallicum 30X, Ferrum Metallicum 8X, Fucus Vesiculosus 3X, Hypericum Perforatum 12X, Kali Phosphoricum 3X, Magnesia Phosphorica 12X, Manganum Metallicum 12X, Mercurius Vivus 12X, Plumbum Metallicum 12X, Silicea 30X, Symphytum Officinale 6X, Tarentula Cubensis 15X, X-Ray 16X, 24X, 30X, Ytterbium Oxide 12X.
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PURPOSE:
Alfalfa – Body Aches, Cadmium Sulphuratum - Nervousness, Calcarea Carbonica – Muscle Cramps, Cuprum Metallicum - Fatigue, Ferrum Metallicum – Body Aches, Fucus Vesiculosus - Nervousness, Hypericum Perforatum – Muscle Cramps, Kali Phosphoricum – Jet Lag, Magnesia Phosphorica – Body Aches, Manganum Metallicum - Nervousness, Mercurius Vivus – Jet Lag, Plumbum Metallicum – Body Aches, Silicea - Nervousness, Symphytum Officinale – Muscle Cramps, Tarentula Cubensis - Fatigue, X-Ray – Jet Lag, Ytterbium Oxide – Body Aches
- USES:
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- DIRECTIONS:
- INACTIVE INGREDIENTS:
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- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
EMF PROTECT AND BALANCE
alfalfa, fucus vesiculosus, kali phosphoricum, symphytum officinale, calcarea carbonica, ferrum metallicum, cadmium sulphuratum, hypericum perforatum, magnesia phosphorica, manganum metallicum, mercurius vivus, plumbum metallicum, ytterbium oxide, tarentula cubensis, x-ray, cuprum metallicum, silicea liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-1594 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD) MEDICAGO SATIVA WHOLE 3 [hp_X] in 1 mL FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X] in 1 mL DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) DIBASIC POTASSIUM PHOSPHATE 3 [hp_X] in 1 mL COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ) COMFREY ROOT 6 [hp_X] in 1 mL OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X] in 1 mL IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7) IRON 8 [hp_X] in 1 mL CADMIUM SULFIDE (UNII: 057EZR4Z7Q) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM SULFIDE 12 [hp_X] in 1 mL HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB) HYPERICUM PERFORATUM WHOLE 12 [hp_X] in 1 mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X] in 1 mL MANGANESE (UNII: 42Z2K6ZL8P) (MANGANESE - UNII:42Z2K6ZL8P) MANGANESE 12 [hp_X] in 1 mL MERCURY (UNII: FXS1BY2PGL) (MERCURY - UNII:FXS1BY2PGL) MERCURY 12 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 12 [hp_X] in 1 mL YTTERBIUM OXIDE (UNII: T66CZ53RP4) (YTTERBIUM OXIDE - UNII:T66CZ53RP4) YTTERBIUM OXIDE 12 [hp_X] in 1 mL CITHARACANTHUS SPINICRUS (UNII: 3Y5X6RT823) (CITHARACANTHUS SPINICRUS - UNII:3Y5X6RT823) CITHARACANTHUS SPINICRUS 15 [hp_X] in 1 mL ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (ALCOHOL, X-RAY EXPOSED (1000 RAD) - UNII:6PRJ93602P) ALCOHOL, X-RAY EXPOSED (1000 RAD) 16 [hp_X] in 1 mL COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5) COPPER 30 [hp_X] in 1 mL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 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:43742-1594-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 01/08/2020 02/27/2028 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/08/2020 02/27/2028 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-1594) , api manufacture(43742-1594) , label(43742-1594) , pack(43742-1594)
