AMALGAM 6003- amalgam liquid

Amalgam by

Drug Labeling and Warnings

Amalgam by is a Homeopathic medication manufactured, distributed, or labeled by Professional Complementary Health Formulas, Natural Pharmaceutical Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Caries 30X, 60X
Gingivitis 30X, 60X
Osteomyelitis 30X, 60X
Periodontitis 30X, 60X
Root ostitis 30X, 60X
and all the following at 30X, 60X, 100X:
Amalgam
Dental gold
Dental plastics
Epoxies
Fluorine
Mercurius solubilis
Misc. binders
Nickel
Palladium
Platinum
Setting agents
Silver (6 types)
Sodium fluoride
Titanium

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of swollen, red, or tender gums, occasional bad breath, minor toothache, occasional headache, irritability, or fatigue due to sensitivity to or exposure to oral/dental materials.*

PURPOSE

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS

Consult a doctor if condition worsens or symptoms persist. Not intended for use by individuals with retained amalgams. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Amalgam

Homeopathic Remedy

2 FL. OZ. (59 mL)

INGREDIENTS AND APPEARANCE

AMALGAM  6003
amalgam liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-6003
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TILLETIA CARIES (UNII: C7000B9PQI) (TILLETIA CARIES - UNII:C7000B9PQI)	TILLETIA CARIES	30 [hp_X]  in 59 mL
BOS TAURUS GINGIVA (UNII: GJ2F3208WP) (BOS TAURUS GINGIVA - UNII:GJ2F3208WP)	BOS TAURUS GINGIVA	30 [hp_X]  in 59 mL
BOS TAURUS BONE (UNII: TRS31EO6ZN) (BOS TAURUS BONE - UNII:TRS31EO6ZN)	BOS TAURUS BONE	30 [hp_X]  in 59 mL
TREPONEMA DENTICOLA (UNII: 6TN2P16IOQ) (TREPONEMA DENTICOLA - UNII:6TN2P16IOQ)	TREPONEMA DENTICOLA	30 [hp_X]  in 59 mL
ISATIS TINCTORIA ROOT (UNII: 8S10GFI6DX) (ISATIS TINCTORIA ROOT - UNII:8S10GFI6DX)	ISATIS TINCTORIA ROOT	30 [hp_X]  in 59 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	30 [hp_X]  in 59 mL
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	30 [hp_X]  in 59 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	30 [hp_X]  in 59 mL
EPICHLOROHYDRIN (UNII: 08OOR508C0) (EPICHLOROHYDRIN - UNII:08OOR508C0)	EPICHLOROHYDRIN	30 [hp_X]  in 59 mL
FLUORINE (UNII: 284SYP0193) (FLUORINE - UNII:284SYP0193)	FLUORINE	30 [hp_X]  in 59 mL
MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2)	MERCURIUS SOLUBILIS	30 [hp_X]  in 59 mL
XANTHAN GUM (UNII: TTV12P4NEE) (XANTHAN GUM - UNII:TTV12P4NEE)	XANTHAN GUM	30 [hp_X]  in 59 mL
NICKEL (UNII: 7OV03QG267) (NICKEL - UNII:7OV03QG267)	NICKEL	30 [hp_X]  in 59 mL
PALLADIUM (UNII: 5TWQ1V240M) (PALLADIUM - UNII:5TWQ1V240M)	PALLADIUM	30 [hp_X]  in 59 mL
PLATINUM (UNII: 49DFR088MY) (PLATINUM - UNII:49DFR088MY)	PLATINUM	30 [hp_X]  in 59 mL
ZINC CATION (UNII: 13S1S8SF37) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	30 [hp_X]  in 59 mL
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	30 [hp_X]  in 59 mL
TITANIUM (UNII: D1JT611TNE) (TITANIUM - UNII:D1JT611TNE)	TITANIUM	30 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63083-6003-2	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/1984

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Pharmaceutical Manufacturing LLC		015624923	manufacture(63083-6003)