Home NDC 43857-0500-1 Lymph
Product NDC 43857-0500
Requested package NDC 43857-0500-1
11-digit product format 438570500
Labeler code 43857
Product ID 43857-0500_f0ada671-af38-4824-a55e-6389ac8f9bf1
Type HUMAN OTC DRUG
Nonproprietary name Echinacea (Angustifolia), Collinsonia Canadensis, Phytolacca Decandra, Kali Iodatum, Pinus Sylvestris, Pix Liquida, Ferrum Phosphoricum, Aesculus Hippocastanum, Baryta Carbonica, Berberis Vulgaris, Calcarea Carbonica, Calcarea Phosphorica, Causticum, Hepar Sulphuris Calcareum, Kreosotum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Nitricum Acidum, Phosphorus, Pulsatilla (Vulgaris), Silicea, Stellaria Media, Sulphur, Terebinthina, Thuja Occidentalis, Bufo Rana
Dosage form LIQUID
Route ORAL
Labeler BioActive Nutritional, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-05-24
Marketing end 2024-07-30
Substance ECHINACEA ANGUSTIFOLIA; COLLINSONIA CANADENSIS ROOT; PHYTOLACCA AMERICANA ROOT; POTASSIUM IODIDE; PINUS SYLVESTRIS LEAFY TWIG; PINE TAR; FERROSOFERRIC PHOSPHATE; HORSE CHESTNUT; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; CAUSTICUM; CALCIUM SULFIDE; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; SODIUM CHLORIDE; NITRIC ACID; PHOSPHORUS; ANEMONE PULSATILLA; SILICON DIOXIDE; STELLARIA MEDIA; SULFUR; TURPENTINE OIL; THUJA OCCIDENTALIS LEAFY TWIG; BUFO BUFO CUTANEOUS GLAND
Active strength 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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 · 11 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…
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 43857-0500-1 43857050001 60 mL in 1 BOTTLE, DROPPER (43857-0500-1) 60 ml 2019-05-24 2024-07-30 No No Current