Home NDC 50845-0254-2 Sinus Congestion Headache
Product NDC 50845-0254
Requested package NDC 50845-0254-2
11-digit product format 508450254
Labeler code 50845
Product ID 50845-0254_c31eec3e-2616-40e9-9437-c5e81f5be1e6
Type HUMAN OTC DRUG
Nonproprietary name Antimonium Tartaricum, Asafoetida, Baptisia Tinctoria, Echinacea (Angustifolia), Eupatorium Perfoliatum, Euphorbia Pilulifera, Hepar Sulphuris Calcareum, Hydrastis Canadensis, Iodium, Kali Bichromicum, Lachesis Mutus, Magnesia Carbonica, Mucosa Nasalis Suis, Pulsatilla (Vulgaris), Pyrogenium, Silicea, Teucrium Marum
Dosage form SPRAY
Route ORAL
Labeler Liddell Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-04-24
Marketing end 2024-06-30
Substance ANTIMONY POTASSIUM TARTRATE; ASAFETIDA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA HIRTA FLOWERING TOP; CALCIUM SULFIDE; GOLDENSEAL; IODINE; POTASSIUM DICHROMATE; LACHESIS MUTA VENOM; MAGNESIUM CARBONATE; SUS SCROFA NASAL MUCOSA; ANEMONE PULSATILLA; RANCID BEEF; SILICON DIOXIDE; TEUCRIUM MARUM
Active strength 6 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/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…
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 50845-0254-2 50845025402 1 BOTTLE, SPRAY in 1 PACKAGE (50845-0254-2) > 30 mL in 1 BOTTLE, SPRAY (50845-0254-1) 2019-04-24 2024-06-30 No No Current