Home NDC 63083-4028-2 Shingles Nosode
Product NDC 63083-4028
Requested package NDC 63083-4028-2
11-digit product format 630834028
Labeler code 63083
Product ID 63083-4028_a45a894a-e945-4f1f-81d1-9490db8da397
Type HUMAN OTC DRUG
Nonproprietary name Shingles Nosode
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ECHINACEA ANGUSTIFOLIA WHOLE; LYSINE; DAPHNE MEZEREUM BARK; TOXICODENDRON PUBESCENS LEAF; SODIUM CHLORIDE; CROTON TIGLIUM SEED; HUMAN HERPESVIRUS 1; RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN; HUMAN VARICELLA-ZOSTER IMMUNE GLOBULIN
Active strength 6; 6; 6; 6; 6; 8; 200; 200; 200 [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
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 Shingles Nosode
Brand name suffix 4028
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA WHOLE 6 [hp_X]/59mL LYSINE 6 [hp_X]/59mL DAPHNE MEZEREUM BARK 6 [hp_X]/59mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/59mL SODIUM CHLORIDE 6 [hp_X]/59mL CROTON TIGLIUM SEED 8 [hp_X]/59mL HUMAN HERPESVIRUS 1 200 [hp_X]/59mL RECOMBINANT VARICELLA ZOSTER VIRUS GLYCOPROTEIN E ANTIGEN 200 [hp_X]/59mL HUMAN VARICELLA-ZOSTER IMMUNE GLOBULIN 200 [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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 N28 2026-01-09 N28 2024-01-30 N28 2024-01-30 N28
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-4028-2 Shingles Nosode4028 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 63083-4028 SHINGLES NOSODE 4028 (SHINGLES NOSODE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220301_e71d917a-af9f-41e9-a3de-cb588db7e022.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 63083-4028-2 63083402802 59 mL in 1 BOTTLE, DROPPER (63083-4028-2) 59 ml 1985-08-15 0000-00-00 No No Current