Home NDC 63083-4004 Vaccinosis Nosode
Product NDC 63083-4004
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 ANGUILLA ROSTRATA BLOOD SERUM; CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED); DIPHENYLTRICHLOROETHANE; LAURTRIMONIUM BROMIDE; MUMPS VIRUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SERUM, HORSE; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAF
Active strength 30; 30; 30; 30; 30; 6; 30; 6; 6 [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 openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 30 [hp_X]/59mL SILICON DIOXIDE 30 [hp_X]/59mL THUJA OCCIDENTALIS LEAF 30 [hp_X]/59mL DIPHENYLTRICHLOROETHANE 30 [hp_X]/59mL LAURTRIMONIUM BROMIDE 30 [hp_X]/59mL MUMPS VIRUS 6 [hp_X]/59mL ANGUILLA ROSTRATA BLOOD SERUM 30 [hp_X]/59mL SERUM, HORSE 6 [hp_X]/59mL CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) 6 [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# 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
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