Bruise

Manufacturer
Remedies Cure, LLC | Apotheca Company
Effective date
2022-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:17:58

Label at a glance#

ProductBruise RX
Active ingredientERIGERON CANADENSIS WHOLE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, PHOSPHORUS, SULFURIC ACID, ARNICA MONTANA WHOLE, RHODODENDRON TOMENTOSUM LEAFY TWIG, BELLIS PERENNIS WHOLE
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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

INDICATIONS:

OTC - PURPOSE SECTION

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:

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INDICATIONS & USAGE SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized Water, Ethanol 20%.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Remedies Cure, LLC

841 Sunset Drive

Kaysville, UT 84037

www.bruiserx.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RemediesCure

Bruise RX

HOMEOPATHIC

1 fl. oz. (30 ml)

Bruise RXBruise RX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82734-0001-1BruiseRX30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82734-0001BRUISE RX (ERIGERON CANADENSIS, HAMAMELIS VIRGINIANA, PHOSPHORUS, SULPHURICUM ACIDUM, ARNICA MONTANA, LEDUM PALUSTRE, BELLIS PERENNIS) LIQUID [REMEDIES CURE, LLC]1Current NDC, Legacy NDC, 1 package rows20220811_8fbac9c7-45ac-4a9b-bdff-6f19d238a601.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82734-000182734-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bruise RXERIGERON CANADENSIS, HAMAMELIS VIRGINIANA, PHOSPHORUS, SULPHURICUM ACIDUM, ARNICA MONTANA, LEDUM PALUSTRE, BELLIS PERENNISRemedies Cure, LLC8fbac9c7-45ac-4a9b-bdff-6f19d238a6012022-08-10WarningsExact identifier
ndc (package): 82734-0001-1
ndc (product): 82734-0001
ndc11 (package): 82734000101
spl id: f7b9f15a-d9a4-4ab8-a993-41c7565344cf
spl set id: 8fbac9c7-45ac-4a9b-bdff-6f19d238a601

Reported adverse events (FAERS/openFDA)#

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