FDA.reportPublic FDA data

TRIDERMA EVERYDAY BRUISE RELIEF

Product NDC
10738-059
11-digit product format
107380059
Labeler code
10738
Product ID
10738-059_497d62b9-309b-5d55-e063-6294a90a7e41
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA
Dosage form
CREAM
Route
TOPICAL
Labeler
Genuine Virgin Aloe Corporation
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-08-30
Substance
ARNICA MONTANA
Active strength
1.6 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
TRIDERMA EVERYDAY BRUISE RELIEF
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA1.6 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
5100f2d0-cfa2-4136-bda4-860de81707c8Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
10738-059-202023-02-02TRIDERMA Everyday Bruise Relief
10738-059-412023-02-02TRIDERMA Everyday Bruise Relief
10738-059-502023-02-02TRIDERMA Everyday Bruise Relief
10738-059-202023-01-30TRIDERMA Everyday Bruise Relief
10738-059-412023-01-30TRIDERMA Everyday Bruise Relief
10738-059-502023-01-30TRIDERMA Everyday Bruise Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10738-059-20TRIDERMA EVERYDAY BRUISE RELIEF1 in 1 CARTONCREAM16
10738-059-25TRIDERMA EVERYDAY BRUISE RELIEF62 g in 1 TUBECREAM626
10738-059-41TRIDERMA EVERYDAY BRUISE RELIEF113 g in 1 JARCREAM1136
10738-059-50TRIDERMA EVERYDAY BRUISE RELIEF1 in 1 CARTONCREAM16
10738-059-55TRIDERMA EVERYDAY BRUISE RELIEF14 g in 1 TUBECREAM146

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10738-059TRIDERMA EVERYDAY BRUISE RELIEF (ARNICA MONTANA) CREAM [GENUINE VIRGIN ALOE CORPORATION]5Current NDC, Legacy NDC, 5 package rows20250101_5100f2d0-cfa2-4136-bda4-860de81707c8.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
TRIDERMA EVERYDAY BRUISE RELIEFARNICA MONTANAGenuine Virgin Aloe Corporation5100f2d0-cfa2-4136-bda4-860de81707c82026-01-28WarningsExact identifier
ndc (product): 10738-059

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10738-059-20107380059201 TUBE in 1 CARTON (10738-059-20) / 62 g in 1 TUBE (10738-059-25) 1 tube2019-08-300000-00-00NoNoCurrent
10738-059-251073800592562 g in 1 TUBE62 gHistorical
10738-059-4110738005941113 g in 1 JAR (10738-059-41) 113 g2019-08-300000-00-00NoNoCurrent
10738-059-50107380059501 TUBE in 1 CARTON (10738-059-50) / 14 g in 1 TUBE (10738-059-55) 1 tube2019-08-300000-00-00NoNoCurrent
10738-059-551073800595514 g in 1 TUBE14 gHistorical