Home NDC 50845-0251-1 Snore Defense
Product NDC 50845-0251
Requested package NDC 50845-0251-1
11-digit product format 508450251
Labeler code 50845
Product ID 50845-0251_df521eee-ede6-4a79-96de-ce9b70d4be45
Type HUMAN OTC DRUG
Nonproprietary name Antimonium tartaricum, Carbo vegetabilis, Grindelia (Robusta), Lung suis, Mucosa nasalis suis, Nux vomica, Quebracho, Sticta pulmonaria, Teucrium marum
Dosage form SPRAY
Route ORAL
Labeler Liddell Laboratories
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-04-02
Marketing end 2024-04-02
Substance ANTIMONY POTASSIUM TARTRATE; ACTIVATED CHARCOAL; GRINDELIA HIRSUTULA FLOWERING TOP; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; STRYCHNOS NUX-VOMICA SEED; ASPIDOSPERMA QUEBRACHO-BLANCO BARK; LOBARIA PULMONARIA; TEUCRIUM MARUM
Active strength 200 [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50845-0251-1 50845025101 30 mL in 1 BOTTLE, SPRAY (50845-0251-1) 30 ml 2019-04-02 2024-04-02 No No Current