Home NDC 63479-1412-1 N12
Product NDC 63479-1412
Requested package NDC 63479-1412-1
11-digit product format 634791412
Labeler code 63479
Product ID 63479-1412_ba5fbf07-d92c-2b1d-e053-2995a90a7e52
Type HUMAN OTC DRUG
Nonproprietary name ARSENIC TRIOXIDE, BAPTISIA TINCTORIA ROOT, SUS SCROFA BONE MARROW, BRYONIA ALBA ROOT, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, OLEA EUROPAEA FLOWER, ULEX EUROPAEUS, FLOWER, LACHESIS MUTA VENOM, LEVISTICUM OFFICINALE, TREPONEMIC SKIN CANKER HUMAN
Dosage form SOLUTION/ DROPS
Route SUBLINGUAL
Labeler Apex Energetics Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1997-12-04
Marketing end 0000-00-00
Substance ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BILBERRY; BRYONIA ALBA ROOT; ECHINACEA ANGUSTIFOLIA; ECHINACEA PURPUREA; GONORRHEAL URETHRAL SECRETION HUMAN; LACHESIS MUTA VENOM; LEVISTICUM OFFICINALE; OLEA EUROPAEA FLOWER; RANCID BEEF; SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI; STAPHYLOCOCCUS EPIDERMIDIS; STAPHYLOCOCCUS HAEMOLYTICUS; STAPHYLOCOCCUS SIMULANS; STREPTOCOCCUS PYOGENES; SULFUR; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; THUJA OCCIDENTALIS LEAFY TWIG; TREPONEMIC SKIN CANKER HUMAN; TUBERCULIN PURIFIED PROTEIN DERIVATIVE; ULEX EUROPAEUS FLOWER; VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN; VISCUM ALBUM FRUITING TOP
Active strength 30 [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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Actively Acquired Immunity [PE], Antigens, Bacterial [CS], Cell-mediated Immunity [PE], Live Vaccinia Virus Vaccine [EPC], Skin Test Antigen [EPC], Smallpox Vaccine [CS], Tuberculosis Skin Test [EPC], Vaccines, Live, Unattenuated [CS]
NDC exclude flag No
Listing certified through 2023-12-31
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 · 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 63479-1412-1 63479141201 30 mL in 1 BOTTLE, GLASS (63479-1412-1) 30 ml 1997-12-04 0000-00-00 No No Current