Home NDC 51393-7656 Gout
Product NDC 51393-7656
11-digit product format 513937656
Labeler code 51393
Product ID 51393-7656_c5752aa4-40c2-4f35-a13f-d5684ec08969
Type HUMAN OTC DRUG
Nonproprietary name Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Leaf
Dosage form SOLUTION/ DROPS
Route TOPICAL
Labeler Forces of Nature
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-02-15
Substance ARNICA MONTANA WHOLE; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF; URTICA URENS WHOLE
Active strength 30; 8; 12; 30 [hp_C]/1000mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/1000mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Gout
Brand name suffix Pain Management
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA WHOLE 30 [hp_C]/1000mL URTICA URENS WHOLE 8 [hp_X]/1000mL SILICON DIOXIDE 12 [hp_X]/1000mL THUJA OCCIDENTALIS LEAF 30 [hp_C]/1000mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51393-7656-1 Gout Pain Management 11 mL in 1 BOTTLE, DISPENSING SOLUTION/ DROPS 11 4 51393-7656-3 Gout Pain Management 30 mL in 1 BOTTLE, DISPENSING SOLUTION/ DROPS 30 4 51393-7656-4 Gout Pain Management 4 mL in 1 BOTTLE, DISPENSING SOLUTION/ DROPS 4 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51393-7656 GOUT PAIN MANAGEMENT (ARNICA MONTANA, URTICA URENS, SILICON DIOXIDE, AND THUJA OCCIDENTALIS LEAF) SOLUTION/ DROPS [FORCES OF NATURE] 3 Current NDC, Legacy NDC, 3 package rows 20221027_9276fe9c-d9a2-4cef-986c-5d7d39f2d6a1.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51393-7656-1 51393765601 11 mL in 1 BOTTLE, DISPENSING (51393-7656-1) 11 ml 2017-02-15 0000-00-00 No No Current 51393-7656-2 51393765602 33 mL in 1 BOTTLE, DISPENSING (51393-7656-2) 33 ml 2017-02-15 0000-00-00 No No Current 51393-7656-3 51393765603 30 mL in 1 BOTTLE, DISPENSING (51393-7656-3) 30 ml 2025-12-01 No No Current 51393-7656-4 51393765604 4 mL in 1 BOTTLE, DISPENSING (51393-7656-4) 4 ml 2017-02-15 0000-00-00 No No Current