FDA.reportPublic FDA data

Arniblend Pain Relief

Product NDC
51393-8200
11-digit product format
513938200
Labeler code
51393
Product ID
51393-8200_5f86c6a8-4fe4-400b-9e72-41c148a55c08
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana Whole, Horse Chestnut, Hypericum Perforatum whole, Ruta Graveolens Flowering Top, and Thuja Occidentalis Leafy Twig
Dosage form
SOLUTION/ DROPS
Route
TOPICAL
Labeler
Forces of Nature
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2025-11-01
Substance
ARNICA MONTANA WHOLE; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; RUTA GRAVEOLENS FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG
Active strength
30; 6; 12; 30; 6 [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_X]/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Arniblend Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE30 [hp_C]/100mL
HORSE CHESTNUT6 [hp_C]/100mL
HYPERICUM PERFORATUM WHOLE12 [hp_C]/100mL
RUTA GRAVEOLENS FLOWERING TOP30 [hp_C]/100mL
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_X]/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO80TY208ZW, 3C18L6RJAZ, XK4IUX8MNB, N94C2U587S, 1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-8200-4Arniblend Pain Relief4 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS41
51393-8200-4Arniblend Pain Relief1 in 1 CARTONSOLUTION/ DROPS11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
51393-8200-4513938200041 BOTTLE, DISPENSING in 1 CARTON (51393-8200-4) / 4 mL in 1 BOTTLE, DISPENSING2025-11-01NoNoCurrent