Home NDC 63083-9402-1 Parasites/Amoeba/Protozoan Nosode Combination
Product NDC 63083-9402
Requested package NDC 63083-9402-1
11-digit product format 630839402
Labeler code 63083
Product ID 63083-9402_ec9e14ed-28bb-4eb1-a7ad-9e4da6fd7eb5
Type HUMAN OTC DRUG
Nonproprietary name Parasites/Amoeba/Protozoan Nosode Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ECHINACEA ANGUSTIFOLIA WHOLE; AMARYLLIS BELLADONNA WHOLE; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM PERFOLIATUM FLOWERING TOP; AMOEBA PROTEUS; ANOPHELES QUADRIMACULATUS; TOXOPLASMA GONDII
Active strength 3; 4; 4; 6; 12; 12; 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 Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC]
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 Parasites/Amoeba/Protozoan Nosode Combination
Brand name suffix 9402
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/29.5mL AMARYLLIS BELLADONNA WHOLE 4 [hp_X]/29.5mL EUCALYPTUS GLOBULUS LEAF 4 [hp_X]/29.5mL EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/29.5mL AMOEBA PROTEUS 12 [hp_X]/29.5mL ANOPHELES QUADRIMACULATUS 12 [hp_X]/29.5mL TOXOPLASMA GONDII 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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 R402 2026-01-09 R402 2024-01-30 R402 2024-01-30 R402
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9402-1 Parasites/Amoeba/Protozoan Nosode Combination9402 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 63083-9402 PARASITES/AMOEBA/PROTOZOAN NOSODE COMBINATION 9402 (PARASITES/AMOEBA/PROTOZOAN NOSODE COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_0846f710-e652-4010-81b6-45a216b0c8c7.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 63083-9402-1 63083940201 29.5 mL in 1 BOTTLE, DROPPER (63083-9402-1) 29.5 ml 1985-08-15 0000-00-00 No No Current