FDA.reportPublic FDA data

BED SORE AND WOUND

Manufacturer
PUREMEDY
Effective date
2024-01-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:25:36

Label at a glance#

ProductBED SORE AND WOUND
Active ingredientARNICA MONTANA, ECHINACEA PURPUREA, CALENDULA OFFICINALIS FLOWER, SAMBUCUS NIGRA FLOWER
Label structure9 sections

Indications and uses

TO RELIEVE SYMPTOMS ASSOCIATED WITH ECZEMA, PSORIASIS, DERMATITIS, SEVIERE DRY, ITCHY FLAKY SKIN

Dosage and administration

APPLY TO AFFECTED AREA 3-4 TIMES PER DAY.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ARNICA MONTANA (ARNICA)

ECHINACEA (PURPLE CONEFLOWER)

CALENDULA OFFICINALIS (MARIGOLD)

SAMBUCUS NIGRA (ELDER FLOWER)

PROPERTIES

OTC - PURPOSE SECTION

REMEDY FOR WOUNDS AND BED SORES

ANTISEPTIC, REMEDY FOR SKIN INFECTION

EXCELLENT REMEDY FOR SKIN HEALING

REMEDY FOR SWELLING

USES

INDICATIONS & USAGE SECTION

TO RELIEVE SYMPTOMS ASSOCIATED WITH ECZEMA, PSORIASIS, DERMATITIS, SEVIERE DRY, ITCHY FLAKY SKIN

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY TO AFFECTED AREA 3-4 TIMES PER DAY.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ORGANIC OLIVE OIL, WILD HARVESTED PINE RESIN, ORGANIC BEESWAX, WILD HARVESTED CANADIAN FIR BALSAM, GMO-FREE ORGANIC VITAMIN E OIL.

WARNING

WARNINGS SECTION

TEST FOR ALLERGY BY RUBBING A SMALL AMOUNT ON SKIN FIRST. DO NOT USE IF ALLERGIC TO OR HYPER-SENSITIVE TO ANY INGREDIENT. IF CONDITION PERSISTS OR WORSENS, CONSULT YOUR HEALTH CARE PROVIDER.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTHER SAFETY INFORMATION

STORE IN A COOL DRY PLACE OR REFRIGERATE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bed Sore-Wound Salve 1oz_LBL_2013-09-08Bed Sore-Wound Salve 1oz_LBL_2013-09-08

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52810-207-122025-07-29C16284748780-13b156c62-2657-fb37-e063-e6dba90a4e07BED SORE AND WOUND SALVE (52810-207)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52810-207-12BED SORE AND WOUND60 mL in 1 JARSALVE604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52810-207BED SORE AND WOUND (ARNICA MONTANA, ECHINACEA, CALENDULA OFFICINALIS, SAMBUSCUS NIGRA) SALVE [PUREMEDY]4Legacy NDC, 1 package rows20240112_721d74b2-82e7-46ee-8b85-54854c2de90e.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52810-20752810-207-12

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OLIVE OIL6UYK2W1W1EIACT
PINE NEEDLE OIL (PINUS SYLVESTRIS)5EXL5H740YIACT
YELLOW WAX2ZA36H0S2VIACT
ABIES BALSAMEA LEAF OIL2FGT9T2SQCIACT
TOCOPHEROLR0ZB2556P8IACT
ARNICA MONTANAO80TY208ZWACTIB
ECHINACEA PURPUREAQI7G114Y98ACTIB
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDACTIB
SAMBUCUS NIGRA FLOWER07V4DX094TACTIB

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
0eb2ec0f-969d-9a70-e063-6294a90abd56721d74b2-82e7-46ee-8b85-54854c2de90e2024-01-11WarningsExact identifier
spl id: 0eb2ec0f-969d-9a70-e063-6294a90abd56
spl set id: 721d74b2-82e7-46ee-8b85-54854c2de90e

Reported adverse events (FAERS/openFDA)#

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