Home NDC 63083-4004-2 Vaccinosis Nosode
Product NDC 63083-4004
Requested package NDC 63083-4004-2
11-digit product format 630834004
Labeler code 63083
Product ID 63083-4004_2edeb83d-2ef5-46ef-898e-93e1e0c40569
Type HUMAN OTC DRUG
Nonproprietary name Vaccinosis Nosode
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF; DIPHENYLTRICHLOROETHANE; LAURTRIMONIUM BROMIDE; MUMPS VIRUS; ANGUILLA ROSTRATA BLOOD SERUM; SERUM, HORSE; CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED)
Active strength 6; 6; 6; 30; 30; 30; 30; 30; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Actively Acquired Immunity [PE], Inactivated Clostridium Tetani Vaccine [EPC], Tetanus Toxoid [CS], Vaccines, Inactivated [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 15 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…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Vaccinosis Nosode
Brand name suffix 4004
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X]/59mL SILICON DIOXIDE 6 [hp_X]/59mL THUJA OCCIDENTALIS LEAF 6 [hp_X]/59mL DIPHENYLTRICHLOROETHANE 30 [hp_X]/59mL LAURTRIMONIUM BROMIDE 30 [hp_X]/59mL MUMPS VIRUS 30 [hp_X]/59mL ANGUILLA ROSTRATA BLOOD SERUM 30 [hp_X]/59mL SERUM, HORSE 30 [hp_X]/59mL CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) 30 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-08 N4 2026-01-08 N4 2024-01-30 N4 2024-01-30 N4
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-4004-2 Vaccinosis Nosode4004 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-4004 VACCINOSIS NOSODE 4004 (VACCINOSIS NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220301_dff675b3-6330-45d0-984c-526a8f44202b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-4004-2 63083400402 59 mL in 1 BOTTLE, DROPPER (63083-4004-2) 59 ml 1985-08-15 0000-00-00 No No Current