Heavy Metal - Amalga Detox

Manufacturer: Newton Laboratories, Inc.
Effective date: 2011-06-01
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:05:22

Label at a glance#

ProductHeavy Metal - Amalga Detox

Active ingredientGarlic, Aluminum, Silver, Gold, Barium Carbonate, Beryllium, Bismuth, Cadmium, Calcium Fluoride, Activated Charcoal, Chelidonium Majus, Cinchona Officinalis Bark, Cobalt, Copper, Glycyrrhiza Glabra, Hydrofluoric Acid, Iris Versicolor Root, Manganese, Mercury, Nickel, Osmium, Platinum, Lead, Tin, Strontium Carbonate, Thallium, Titanium, Silybum Marianum Seed, Taraxacum Officinale

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1.800.448.7256

Websitewww.newtonlabs.net

www.newtonlabs.net

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Heavy Metal - Amalga Detox Formulated for symptoms of heavy metal and amalgam exposure such as fatigue, headaches, compromised immunity and sluggish elimination.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) one to four times daily or as directed by a healthcare professional. Under age 2, crush or dissolve pellets in purified water.

ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Allium sativum 20x, Aluminium metallicum 20x, Arg. met. 20x, Aur. met. 20x, Baryta carb. 20x, Beryllium metallicum 20x, Bismuthum metallicum 20x, Cadmium metallicum 20x, Calc. fluor. 20x, Carbo veg. 20x, Chelidonium majus 20x, Cinchona 20x, Cobaltum met. 20x, Cuprum met. 20x, Glycyrrhiza glabra 20x, Hydrofluoricum acidum 20x, Iris versicolor 20x, Manganum metallicum 20x, Merc. viv. 20x, Niccolum metallicum 20x, Osmium metallicum 20x, Platinum met. 20x, Plumb. met. 20x, Stannum met. 20x, Strontium carb. 20x, Thallium metallicum 20x, Titanium metallicum 20x, Carduus mar. 8x, Iris versicolor 8x, Taraxacum 8x, Carduus mar. 3x, Iris versicolor 3x, Taraxacum 3x.

PURPOSE SECTION

ABUSE SECTION

Formulated for symptoms of heavy metal and amalgam exposure such as fatigue, headaches, compromised immunity and sluggish elimination.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose pellets.

QUESTIONS? SECTION

OTC - QUESTIONS SECTION

www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions? 1.800.448.7256

WARNINGS SECTION

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

PREGNANCY OR BREAST FEEDING SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant or nursing or if symptoms worsen or persist for more than a few days.

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c599c4a0-705d-4ebb-ab1f-977af038f96a	Product name	1	20251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55714-4561-1	2020-01-31	C162847	48780-1	9d75b9d0-1db0-f424-e053-dadaa90a57ce	Heavy Metal - Amalga Detox
55714-4561-2	2020-01-31	C162847	48780-1	9d75b9d0-1db0-f424-e053-dadaa90a57ce	Heavy Metal - Amalga Detox

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55714-4561-1	Heavy Metal - Amalga Detox	28.35 g in 1 BOTTLE, GLASS	PELLET	28.35		1
55714-4561-2	Heavy Metal - Amalga Detox	56.7 g in 1 BOTTLE, GLASS	PELLET	56.7		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55714-4561	HEAVY METAL - AMALGA DETOX (ALLIUM SAT., ALUMIN MET., ARG. MET., AUR. MET., BARYTA CARB., BERYLLIUM, BISMUTHUM MET., CADMIUM MET., CALC. FLUOR., CARBO VEG., CHELIDONIUM MAJ., CINCHONA, COBALTUM MET., CUPRUM MET., GLYCYRRHIZA, HYDROFLUORICUM AC., IRIS VERSICOLOR, MANG MET., MERC. VIV., NICCOLUM MET., OSMIUM MET., PLATINUM MET., PLUMB. MET., STANNUM MET., STRONTIUM CARB., THALLIUM MET., TITANIUM MET., CARDUUS MAR., TARAXACUM) PELLET [NEWTON LABORATORIES, INC.]	1	Legacy NDC, 2 package rows	20140108_89146076-10f8-65e5-e994-d0468948881b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Activated Charcoal	ACTIVE INGREDIENT	2P3VWU3H10	1
Aluminum	ACTIVE INGREDIENT	CPD4NFA903	1
Barium Carbonate	ACTIVE INGREDIENT	6P669D8HQ8	1
Beryllium	ACTIVE INGREDIENT	OW5102UV6N	1
Bismuth	ACTIVE INGREDIENT	U015TT5I8H	1
Cadmium	ACTIVE INGREDIENT	00BH33GNGH	1
Calcium Fluoride	ACTIVE INGREDIENT	O3B55K4YKI	1
Chelidonium Majus	ACTIVE INGREDIENT	7E889U5RNN	1
Cinchona Officinalis Bark	ACTIVE INGREDIENT	S003A158SB	1
Cobalt	ACTIVE INGREDIENT	3G0H8C9362	1
Copper	ACTIVE INGREDIENT	789U1901C5	1
Garlic	ACTIVE INGREDIENT	V1V998DC17	1
Glycyrrhiza Glabra	ACTIVE INGREDIENT	2788Z9758H	1
Gold	ACTIVE INGREDIENT	79Y1949PYO	1
Hydrofluoric Acid	ACTIVE INGREDIENT	RGL5YE86CZ	1
Iris Versicolor Root	ACTIVE INGREDIENT	X43D4L3DQC	1
Lead	ACTIVE INGREDIENT	2P299V784P	1
Manganese	ACTIVE INGREDIENT	42Z2K6ZL8P	1
Mercury	ACTIVE INGREDIENT	FXS1BY2PGL	1
Nickel	ACTIVE INGREDIENT	7OV03QG267	1
Osmium	ACTIVE INGREDIENT	2E7M255OPY	1
Platinum	ACTIVE INGREDIENT	49DFR088MY	1
Silver	ACTIVE INGREDIENT	3M4G523W1G	1
Silybum Marianum Seed	ACTIVE INGREDIENT	U946SH95EE	1
Strontium Carbonate	ACTIVE INGREDIENT	41YPU4MMCA	1
Taraxacum Officinale	ACTIVE INGREDIENT	39981FM375	1
Thallium	ACTIVE INGREDIENT	AD84R52XLF	1
Tin	ACTIVE INGREDIENT	387GMG9FH5	1
Titanium	ACTIVE INGREDIENT	D1JT611TNE	1
Activated Charcoal	ACTIVE MOIETY	2P3VWU3H10	1
Aluminum	ACTIVE MOIETY	CPD4NFA903	1
Barium Cation	ACTIVE MOIETY	V645272HLN	1
Beryllium	ACTIVE MOIETY	OW5102UV6N	1
Bismuth	ACTIVE MOIETY	U015TT5I8H	1
Cadmium	ACTIVE MOIETY	00BH33GNGH	1
Chelidonium Majus	ACTIVE MOIETY	7E889U5RNN	1
Cinchona Officinalis Bark	ACTIVE MOIETY	S003A158SB	1
Cobalt	ACTIVE MOIETY	3G0H8C9362	1
Copper	ACTIVE MOIETY	789U1901C5	1
Fluoride Ion	ACTIVE MOIETY	Q80VPU408O	1
Garlic	ACTIVE MOIETY	V1V998DC17	1
Glycyrrhiza Glabra	ACTIVE MOIETY	2788Z9758H	1
Gold	ACTIVE MOIETY	79Y1949PYO	1
Iris Versicolor Root	ACTIVE MOIETY	X43D4L3DQC	1
Lead	ACTIVE MOIETY	2P299V784P	1
Manganese	ACTIVE MOIETY	42Z2K6ZL8P	1
Mercury	ACTIVE MOIETY	FXS1BY2PGL	1
Nickel	ACTIVE MOIETY	7OV03QG267	1
Osmium	ACTIVE MOIETY	2E7M255OPY	1
Platinum	ACTIVE MOIETY	49DFR088MY	1
Silver	ACTIVE MOIETY	3M4G523W1G	1
Silybum Marianum Seed	ACTIVE MOIETY	U946SH95EE	1
Strontium Cation	ACTIVE MOIETY	37077S2C93	1
Taraxacum Officinale	ACTIVE MOIETY	39981FM375	1
Thallium	ACTIVE MOIETY	AD84R52XLF	1
Tin	ACTIVE MOIETY	387GMG9FH5	1
Titanium	ACTIVE MOIETY	D1JT611TNE	1
Sucrose	INACTIVE INGREDIENT	C151H8M554	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 35 matching rows.

Heavy Metal - Amalga Detox
Allium sat., Alumin met., Arg. met., Aur. met., Baryta carb., Beryllium, Bismuthum met., Cadmium met., Calc. fluor., Carbo veg., Chelidonium maj., Cinchona, Cobaltum met., Cuprum met., Glycyrrhiza, Hydrofluoricum ac., Iris versicolor, Mang met., Merc. viv., Niccolum met., Osmium met., Platinum met., Plumb. met., Stannum met., Strontium carb., Thallium met., Titanium met., Carduus mar., Taraxacum
Garlic
Aluminum
Silver
Gold
Barium Carbonate
Barium Cation
Beryllium
Bismuth
Cadmium
Calcium Fluoride
Fluoride Ion
Activated Charcoal
Chelidonium Majus
Cinchona Officinalis Bark
Cobalt
Copper
Glycyrrhiza Glabra
Hydrofluoric Acid
Iris Versicolor Root
Manganese
Mercury
Nickel
Osmium
Platinum
Lead
Tin
Strontium Carbonate
Strontium Cation
Thallium
Titanium
Silybum Marianum Seed
Taraxacum Officinale
Sucrose

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-4561	55714-4561-1, 55714-4561-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Garlic	V1V998DC17	ACTIB
Aluminum	CPD4NFA903	ACTIB
Silver	3M4G523W1G	ACTIB
Gold	79Y1949PYO	ACTIB
Barium Carbonate	6P669D8HQ8	ACTIB
Beryllium	OW5102UV6N	ACTIB
Bismuth	U015TT5I8H	ACTIB
Cadmium	00BH33GNGH	ACTIB
Calcium Fluoride	O3B55K4YKI	ACTIB
Activated Charcoal	2P3VWU3H10	ACTIB
Chelidonium Majus	7E889U5RNN	ACTIB
Cinchona Officinalis Bark	S003A158SB	ACTIB
Cobalt	3G0H8C9362	ACTIB
Copper	789U1901C5	ACTIB
Glycyrrhiza Glabra	2788Z9758H	ACTIB
Hydrofluoric Acid	RGL5YE86CZ	ACTIM
Iris Versicolor Root	X43D4L3DQC	ACTIB
Manganese	42Z2K6ZL8P	ACTIB
Mercury	FXS1BY2PGL	ACTIB
Nickel	7OV03QG267	ACTIB
Osmium	2E7M255OPY	ACTIB
Platinum	49DFR088MY	ACTIB
Lead	2P299V784P	ACTIB
Tin	387GMG9FH5	ACTIB
Strontium Carbonate	41YPU4MMCA	ACTIB
Thallium	AD84R52XLF	ACTIB
Titanium	D1JT611TNE	ACTIB
Silybum Marianum Seed	U946SH95EE	ACTIB
Taraxacum Officinale	39981FM375	ACTIB
Sucrose	C151H8M554	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 48 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Sucrose	SUCROSE	C151H8M554	DROPS / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	WAFER / ORAL	155.2 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, EMULSION / INTRAVENOUS		970 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, FILM COATED / ORAL		145 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SYRUP / ORAL		46400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL		18790 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / TRANSMUCOSAL		1255 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE / ORAL		3568 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS		1 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LIQUID / ORAL		37500 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS	9.4 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SOLUTION / ORAL		42596 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION, EXTENDED RELEASE / ORAL		5400 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, DELAYED RELEASE / ORAL	295.33 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	LOZENGE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / BUCCAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / SUBCUTANEOUS	47.75 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	GRANULE, FOR SUSPENSION / ORAL		31885 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CONCENTRATE / ORAL		4800 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / RECTAL	35.42 %w/v		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUPPOSITORY / RECTAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / ORAL		4249 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, COATED PELLETS / ORAL	59.8 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / BUCCAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION/ DROPS / ORAL		3750 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, EXTENDED RELEASE / ORAL		619 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTABLE, LIPOSOMAL / INTRAVENOUS		7560 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	PASTILLE / ORAL	426 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, DELAYED RELEASE / ORAL		955 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SOLUTION / ORAL		70000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	SUSPENSION / ORAL		48209 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, COATED / ORAL	516.42 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SUSPENSION / ORAL		40017 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS		308 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, CHEWABLE / ORAL		7258 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS	900 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	ELIXIR / ORAL		18000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, SOLUTION / INTRAVENOUS	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, EXTENDED RELEASE / ORAL	284.54 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	CAPSULE, COATED, EXTENDED RELEASE / ORAL		86 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION / INTRAVENOUS		1950 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS		2000 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER, FOR SOLUTION / ORAL		38666 mg	Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TROCHE / ORAL	NA		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	119.12 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	TABLET / SUBLINGUAL	109 mg		Exact identifier — unii candidate 48 equally ranked IID candidates
Sucrose	SUCROSE	C151H8M554	POWDER / ORAL		27768 mg	Exact identifier — unii candidate 48 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5ae84d1d-d38f-4150-5601-8165ff09bd83			89146076-10f8-65e5-e994-d0468948881b	2011-06-01	Warnings	Exact identifier spl id: 5ae84d1d-d38f-4150-5601-8165ff09bd83 spl set id: 89146076-10f8-65e5-e994-d0468948881b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.