Arnicare Bruise

Product NDC
0220-9085
11-digit product format
002209085
Labeler code
0220
Product ID
0220-9085_52438e93-1ee7-5f08-e063-6394a90a4415
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA
Dosage form
CREAM
Route
TOPICAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-01-21
Substance
ARNICA MONTANA
Active strength
1 [hp_X]/[hp_X]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arnicare Bruise
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA1 [hp_X]/[hp_X]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9085-60Arnicare Bruise1 [hp_X] in 1 TUBECREAM19
0220-9085-60Arnicare Bruise1 in 1 PACKAGECREAM19
0220-9085-63Arnicare Bruise1 [hp_X] in 1 TUBECREAM19
0220-9085-63Arnicare Bruise1 in 1 CARTONCREAM19
0220-9085-82Arnicare Bruise1 [hp_X] in 1 TUBECREAM19
0220-9085-82Arnicare Bruise1 in 1 CARTONCREAM19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9085ARNICARE BRUISE (ARNICA MONTANA) CREAM [BOIRON]6Current NDC, Legacy NDC, 6 package rows20250108_b957a592-e51b-61fc-e053-2995a90aaabd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-9085-60002209085601 TUBE in 1 PACKAGE (0220-9085-60) / 1 [hp_X] in 1 TUBE1 tube2021-01-210000-00-00NoNoCurrent
0220-9085-63002209085631 TUBE in 1 CARTON (0220-9085-63) / 1 [hp_X] in 1 TUBE1 tube2024-01-03NoNoCurrent
0220-9085-82002209085821 TUBE in 1 CARTON (0220-9085-82) / 1 [hp_X] in 1 TUBE1 tube2024-01-03NoNoCurrent