Home NDC 63083-9318-1 Nitro-Thio Combination
Product NDC 63083-9318
Requested package NDC 63083-9318-1
11-digit product format 630839318
Labeler code 63083
Product ID 63083-9318_f8083cbc-28e5-4a2d-b5bc-01175901e669
Type HUMAN OTC DRUG
Nonproprietary name Nitro-Thio Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ALDICARB; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CHELIDONIUM MAJUS WHOLE; DNOC; GELSEMIUM SEMPERVIRENS ROOT; PROPINEB; STRYCHNOS NUX-VOMICA SEED
Active strength 12; 10; 3; 10; 12; 3; 12; 6 [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; [hp_X]/29.5mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [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 Nitro-Thio Combination
Brand name suffix 9318
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BLACK COHOSH 12 [hp_X]/29.5mL GELSEMIUM SEMPERVIRENS ROOT 10 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 3 [hp_X]/29.5mL BERBERIS VULGARIS ROOT BARK 10 [hp_X]/29.5mL CHELIDONIUM MAJUS WHOLE 12 [hp_X]/29.5mL ALDICARB 3 [hp_X]/29.5mL DNOC 12 [hp_X]/29.5mL PROPINEB 6 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 R318 2026-01-09 R318 2024-01-30 R318 2024-01-30 R318
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9318-1 Nitro-Thio Combination9318 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 63083-9318 NITRO-THIO COMBINATION 9318 (NITRO-THIO COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_8ef8ac5a-df80-43a7-827d-de224a19beb9.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 63083-9318-1 63083931801 29.5 mL in 1 BOTTLE, DROPPER (63083-9318-1) 29.5 ml 1985-08-15 0000-00-00 No No Current