Bruise

Product NDC
82734-0001
11-digit product format
827340001
Labeler code
82734
Product ID
82734-0001_f7b9f15a-d9a4-4ab8-a993-41c7565344cf
Type
HUMAN OTC DRUG
Nonproprietary name
Erigeron Canadensis, Hamamelis Virginiana, Phosphorus, Sulphuricum Acidum, Arnica Montana, Ledum Palustre, Bellis Perennis
Dosage form
LIQUID
Route
ORAL
Labeler
Remedies Cure, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-08-10
Substance
ERIGERON CANADENSIS WHOLE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PHOSPHORUS; SULFURIC ACID; ARNICA MONTANA WHOLE; RHODODENDRON TOMENTOSUM LEAFY TWIG; BELLIS PERENNIS WHOLE
Active strength
30; 6; 6; 9; 12; 12; 30 [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Bruise
Brand name suffix
RX
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ERIGERON CANADENSIS WHOLE30 [hp_X]/mL
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK6 [hp_C]/mL
PHOSPHORUS6 [hp_C]/mL
SULFURIC ACID9 [hp_C]/mL
ARNICA MONTANA WHOLE12 [hp_C]/mL
RHODODENDRON TOMENTOSUM LEAFY TWIG12 [hp_C]/mL
BELLIS PERENNIS WHOLE30 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
16D08B0B9NInternal UNII lookup
T7S323PKJSInternal UNII lookup
27YLU75U4WInternal UNII lookup
O40UQP6WCFInternal UNII lookup
O80TY208ZWInternal UNII lookup
877L01IZ0PInternal UNII lookup
2HU33I03UYInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8fbac9c7-45ac-4a9b-bdff-6f19d238a601Available on FDA.report

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

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 (product): 82734-0001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82734-0001-18273400010130 mL in 1 BOTTLE, DROPPER (82734-0001-1) 30 ml2022-08-100000-00-00NoNoCurrent