Home NDC 59985-310-32 REMEDI Health Solutions
Product NDC 59985-310
Requested package NDC 59985-310-32
11-digit product format 599850310
Labeler code 59985
Product ID 59985-310_b0c9cd55-32d0-49da-b4db-ebbd41ad1e83
Type HUMAN OTC DRUG
Nonproprietary name ALUMINUM OXIDE, AMYLENUM NITROSUM, ARGENTUM NITRICUM, ARSENICUM IODATUM, CALENDULA OFFICINALIS, CONIUM MACULATUM, EUPHRASIA OFFICINALIS, PHYSOSTIGMA VENENOSUM, RUTA GRAVEOLENS
Dosage form SPRAY
Route ORAL
Labeler Chc Montana
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-01-01
Marketing end 0000-00-00
Substance ALUMINUM OXIDE; AMYL NITRITE; SILVER NITRATE; ARSENIC TRIIODIDE; CALENDULA OFFICINALIS FLOWERING TOP; CONIUM MACULATUM FLOWERING TOP; EUPHRASIA STRICTA; PHYSOSTIGMA VENENOSUM SEED; RUTA GRAVEOLENS FLOWERING TOP
Active strength 6 [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 8 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2024-11-09 02:27 UTC · source 2024-11-08 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59985-310 REMEDI HEALTH SOLUTIONS IRRITABLE EYE RELIEF (ALUMINUM OXIDE, AMYLENUM NITROSUM, ARGENTUM NITRICUM, ARSENICUM IODATUM, CALENDULA OFFICINALIS, CONIUM MACULATUM, EUPHRASIA OFFICINALIS, PHYSOSTIGMA VENENOSUM, RUTA GRAVEOLENS) SPRAY [CHC MONTANA] 4 Legacy NDC 20241205_e931de06-9d2f-45d9-8350-ce7205fb50e0.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 59985-310-32 59985031032 1 BOTTLE, SPRAY in 1 BOX (59985-310-32) > 30 mL in 1 BOTTLE, SPRAY 2019-01-01 0000-00-00 No No Current