BIOPLASMA- calcium fluoride, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, potassium phosphate, dibasic, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium chloride, sodium phosphate, dibasic, heptahydrate, sodium sulfate, and silicon dioxide tablet, soluble

Bioplasma by

Drug Labeling and Warnings

Bioplasma by is a Homeopathic medication manufactured, distributed, or labeled by Hyland's Inc., Merical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

For relief of symptoms of colds, simple nervous tension, fatigue and headaches.

PURPOSE

For relief of symptoms of colds, simple nervous tension, fatigue and headaches

ACTIVE INGREDIENT

Calc Fluor 6X HPUS, Calc Phos 3X HPUS, Calc Sulph 3X HPUS, Ferrum Phos 3X HPUS, Kali Mur 3X HPUS, Kali Phos 3X HPUS, Kali Sulph 3X HPUS, Mag Phos 3X HPUS, Nat Mur 6X HPUS, Nat Phos 3X HPUS, Nat Sulphuricum 3X HPUS, Silicea 6X HPUS

“HPUS” indicates that the active ingredients are in the official Homeopathic Pharmacopœia of the United States.

Directions

Adults & Children ages 7 - 12 years: 4 tablets. Children ages 2 - 6 years: 2 tablets. Dissolve under tongue 3 times a day. Use more frequently (every 15 minutes Manufactured for: for up to 8 doses) with acute conditions.

Warnings

Do not use if imprinted cap band is broken or missing.

If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product.

If symptoms persist for more than seven days or worsen, contact a licensed health care provider.

Keep all medications out of the reach of children.

INACTIVE INGREDIENT

Acacia Gum, Lactose N.F.

PRINCIPAL DISPLAY PANEL - 1000 TABLET BOTTLE LABEL

NDC: 54973-1068-2

HOMEOPATHIC

SINCE 1903

Hyland's®

Bioplasma ®

A combination of all

Twelve Cell Salts

For relief of symptoms of colds, simple

nervous tension,fatigue

and headaches*

1000 TABLETS

INGREDIENTS AND APPEARANCE

BIOPLASMA 
calcium fluoride, tribasic calcium phosphate, calcium sulfate anhydrous, ferrosoferric phosphate, potassium chloride, potassium phosphate, dibasic, potassium sulfate, magnesium phosphate, dibasic trihydrate, sodium chloride, sodium phosphate, dibasic, heptahydrate, sodium sulfate, and silicon dioxide tablet, soluble

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54973-1068
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)	CALCIUM FLUORIDE	6 [hp_X]
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CATION	3 [hp_X]
CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE ANHYDROUS	3 [hp_X]
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7)	FERROSOFERRIC PHOSPHATE	3 [hp_X]
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	3 [hp_X]
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR)	POTASSIUM PHOSPHATE, DIBASIC	3 [hp_X]
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG)	POTASSIUM SULFATE	3 [hp_X]
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE	3 [hp_X]
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6 [hp_X]
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR)	SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE	3 [hp_X]
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)	SODIUM SULFATE	3 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54973-1068-6	8 in 1 PACKET; Type 0: Not a Combination Product	01/01/1940
2	NDC: 54973-1068-1	500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940
3	NDC: 54973-1068-2	1000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/1940

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/1940

Labeler - Hyland's (028570695)

Establishment
Name	Address	ID/FEI	Business Operations
Standard Homeopathic Company		008316655	manufacture(54973-1068)

Establishment
Name	Address	ID/FEI	Business Operations
Merical, Inc.		118445308	manufacture(54973-1068)