BRUISE RX- erigeron canadensis, hamamelis virginiana, phosphorus, sulphuricum acidum, arnica montana, ledum palustre, bellis perennis liquid

Bruise by

Drug Labeling and Warnings

Bruise by is a Homeopathic medication manufactured, distributed, or labeled by Remedies Cure, LLC, Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Erigeron Canadensis 30X, Hamamelis Virginiana 6C, Phosphorus 6C, Sulphuricum Acidum 9C, Arnica Montana 12C, Ledum Palustre 12C, Bellis Perennis 30C.

INDICATIONS:

May aid in the resolution of bruising caused by cosmetic injections, minor surgery and minor trauma.**

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

WARNINGS:

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

KEEP OUT OF REACH OF CHILDREN.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Take 15 drops in small amounts of water by mouth 3 times a day or as directed by a health professional. Children under 12: Take half the adulf dose. Consult a physician for use in children under 12 years of age. If symptoms persist ore worsen, consult a health professional.

INDICATIONS:

May aid in the resolution of bruising caused by cosmetic injections, minor surgery and minor trauma.**

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

INACTIVE INGREDIENTS:

Demineralized Water, Ethanol 20%.

QUESTIONS:

Dist. By: Remedies Cure, LLC

841 Sunset Drive

Kaysville, UT 84037

www.bruiserx.com

PACKAGE LABEL DISPLAY:

RemediesCure

Bruise RX

HOMEOPATHIC

1 fl. oz. (30 ml)

INGREDIENTS AND APPEARANCE

BRUISE  RX
erigeron canadensis, hamamelis virginiana, phosphorus, sulphuricum acidum, arnica montana, ledum palustre, bellis perennis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82734-0001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ERIGERON CANADENSIS WHOLE (UNII: 16D08B0B9N) (ERIGERON CANADENSIS - UNII:16D08B0B9N)	ERIGERON CANADENSIS WHOLE	30 [hp_X]  in 1 mL
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - UNII:T7S323PKJS)	HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK	6 [hp_C]  in 1 mL
PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	PHOSPHORUS	6 [hp_C]  in 1 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)	SULFURIC ACID	9 [hp_C]  in 1 mL
ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA WHOLE	12 [hp_C]  in 1 mL
RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	RHODODENDRON TOMENTOSUM LEAFY TWIG	12 [hp_C]  in 1 mL
BELLIS PERENNIS WHOLE (UNII: 2HU33I03UY) (BELLIS PERENNIS - UNII:2HU33I03UY)	BELLIS PERENNIS WHOLE	30 [hp_C]  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: 82734-0001-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/10/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/10/2022

Labeler - Remedies Cure, LLC (117433850)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(82734-0001) , api manufacture(82734-0001) , label(82734-0001) , pack(82734-0001)