Home NDC 59985-300 Remedi Health Solutions
Product NDC 59985-300
11-digit product format 599850300
Labeler code 59985
Product ID 59985-300_2bf041f2-d289-4bcf-9218-d2f753c83541
Type HUMAN OTC DRUG
Nonproprietary name BOVISTA LYCOPERDON, SECALE CORNUTUM, USTILAGO MAYDIS, WYETHIA HELENIOIDES
Dosage form SPRAY
Route ORAL; TOPICAL
Labeler Chc Montana
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-01-01
Marketing end 0000-00-00
Substance LYCOPERDON UTRIFORME FRUITING BODY; CLAVICEPS PURPUREA SCLEROTIUM; USTILAGO MAYDIS; WYETHIA HELENIOIDES ROOT
Active strength 30 [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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59985-300-32 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59985-300-32 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 59985-300-32 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 59985-300-32 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 59985-300-32 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 59985-300-32 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 59985-300-32 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 59985-300-32 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 59985-300 REMEDI HEALTH SOLUTIONS ALLERGY MOLD, DUST AND HAY (BOVISTA LYCOPERDON, SECALE CORNUTUM, USTILAGO MAYDIS, WYETHIA HELENIOIDES) SPRAY [CHC MONTANA] 4 Legacy NDC 20241205_5feebf0e-96d1-4c81-9383-da31e274a8dd.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 59985-300-32 59985030032 1 BOTTLE, SPRAY in 1 BOX (59985-300-32) > 30 mL in 1 BOTTLE, SPRAY 2019-01-01 0000-00-00 No No Current