Home NDC 63083-9414-1 Pneumonia/Meningitis Nosode Combination
Product NDC 63083-9414
Requested package NDC 63083-9414-1
11-digit product format 630839414
Labeler code 63083
Product ID 63083-9414_788d23ee-d839-48b9-ab74-b66d71e0d630
Type HUMAN OTC DRUG
Nonproprietary name Pneumonia/Meningitis Nosode Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ACONITUM NAPELLUS WHOLE; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; NEISSERIA MENINGITIDIS GROUP A CAPSULAR POLYSACCHARIDE ANTIGEN; SILICON DIOXIDE; SODIUM CARBONATE; STREPTOCOCCUS PYOGENES
Active strength 3; 3; 3; 12; 12; 3; 12 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
Pharmacologic classes Actively Acquired Immunity [PE], Inactivated Meningococcal Vaccine [EPC], Meningococcal Vaccines [CS], Polysaccharides, Bacterial [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…
Additional Listing Data#
Finished product Yes
Brand name base Pneumonia/Meningitis Nosode Combination
Brand name suffix 9414
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS WHOLE 3 [hp_X]/29.5mL BRYONIA ALBA ROOT 3 [hp_X]/29.5mL GELSEMIUM SEMPERVIRENS ROOT 3 [hp_X]/29.5mL SODIUM CARBONATE 12 [hp_X]/29.5mL NEISSERIA MENINGITIDIS GROUP A CAPSULAR POLYSACCHARIDE ANTIGEN 12 [hp_X]/29.5mL STREPTOCOCCUS PYOGENES 3 [hp_X]/29.5mL SILICON DIOXIDE 12 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 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 2026-01-09 R414 2026-01-09 R414 2024-01-30 R414 2024-01-30 R414
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9414-1 Pneumonia/Meningitis Nosode Combination9414 29.5 mL in 1 BOTTLE, DROPPER LIQUID 29.5 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-9414 PNEUMONIA/MENINGITIS NOSODE COMBINATION 9414 (PNEUMONIA/MENINGITIS NOSODE COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_823de3e3-4d20-446c-988d-d7a70a747f9a.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 63083-9414-1 63083941401 29.5 mL in 1 BOTTLE, DROPPER (63083-9414-1) 29.5 ml 1985-08-15 0000-00-00 No No Current