FIBROUS BREAST DROPS 2148- fibrous breast drops liquid

Fibrous Breast Drops by

Drug Labeling and Warnings

Fibrous Breast Drops 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

Echinacea angustifolia 1X
Chamomilla 3X
Phytolacca decandra 4X
Bryonia 6X
Chamomilla 6X
Lymph 6X
Mammary 6X
Cistus canadensis 6X, 12X, 30X
Arnica montana 6X, 12X, 30X, 60X
Aethusa cynapium 12X
Sanguinaria canadensis 12X
Calcarea carbonica 30X
Conium maculatum 30X
Onosmodium virginianum 30X
Psorinum 30X, 60X, 100X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of swollen, tender, sore, or painful breasts.*

PURPOSE

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

WARNINGS

Consult a doctor if condition worsens or if symptoms persist. 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. Not intended for use in infants.

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

Fibrous Breast Drops

Homeopathic Remedy

2 FL. OZ. (59 mL)

INGREDIENTS AND APPEARANCE

FIBROUS BREAST DROPS  2148
fibrous breast drops liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-2148
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA WHOLE - UNII:VB06AV5US8)	ECHINACEA ANGUSTIFOLIA WHOLE	1 [hp_X]  in 59 mL
ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (ARTEMISIA ANNUA FLOWERING TOP - UNII:0UQK6O82OW)	ARTEMISIA ANNUA FLOWERING TOP	3 [hp_X]  in 59 mL
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	4 [hp_X]  in 59 mL
BRYONIA ALBA ROOT (UNII: T7J046YI2B) (BRYONIA ALBA ROOT - UNII:T7J046YI2B)	BRYONIA ALBA ROOT	6 [hp_X]  in 59 mL
BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (BOS TAURUS LYMPH VESSEL - UNII:85I1Z426OV)	BOS TAURUS LYMPH VESSEL	6 [hp_X]  in 59 mL
SUS SCROFA MAMMARY GLAND (UNII: 692OX2DX0E) (SUS SCROFA MAMMARY GLAND - UNII:692OX2DX0E)	SUS SCROFA MAMMARY GLAND	6 [hp_X]  in 59 mL
HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (HELIANTHEMUM CANADENSE - UNII:46G3W789Q3)	HELIANTHEMUM CANADENSE	6 [hp_X]  in 59 mL
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA WHOLE - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	6 [hp_X]  in 59 mL
AETHUSA CYNAPIUM WHOLE (UNII: M6936L953C) (AETHUSA CYNAPIUM WHOLE - UNII:M6936L953C)	AETHUSA CYNAPIUM WHOLE	12 [hp_X]  in 59 mL
SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508)	SANGUINARIA CANADENSIS ROOT	12 [hp_X]  in 59 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	30 [hp_X]  in 59 mL
CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371)	CONIUM MACULATUM FLOWERING TOP	30 [hp_X]  in 59 mL
ONOSMODIUM VIRGINIANUM (UNII: 604NK4250S) (ONOSMODIUM VIRGINIANUM - UNII:604NK4250S)	ONOSMODIUM VIRGINIANUM	30 [hp_X]  in 59 mL
SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (SCABIES LESION LYSATE (HUMAN) - UNII:5UAU16Z1U4)	SCABIES LESION LYSATE (HUMAN)	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: 63083-2148-2	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(63083-2148)