Home NDC 63083-9207-1 Argentum Combination
Product NDC 63083-9207
Requested package NDC 63083-9207-1
11-digit product format 630839207
Labeler code 63083
Product ID 63083-9207_94df6857-aa9b-4647-a19d-67ecf0ffe680
Type HUMAN OTC DRUG
Nonproprietary name Argentum Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AETHUSA CYNAPIUM WHOLE; IPECAC; ROBINIA PSEUDOACACIA BARK; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; COLCHICUM AUTUMNALE BULB; STRYCHNOS IGNATII SEED; IODINE; LIQUID PETROLEUM; CLOSTRIDIUM BOTULINUM; LACHESIS MUTA VENOM; SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI
Active strength 4; 4; 4; 6; 6; 6; 6; 6; 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; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
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 Argentum Combination
Brand name suffix 9207
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AETHUSA CYNAPIUM WHOLE 4 [hp_X]/29.5mL IPECAC 4 [hp_X]/29.5mL ROBINIA PSEUDOACACIA BARK 4 [hp_X]/29.5mL SEMECARPUS ANACARDIUM JUICE 6 [hp_X]/29.5mL SILVER NITRATE 6 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 6 [hp_X]/29.5mL STRYCHNOS IGNATII SEED 6 [hp_X]/29.5mL IODINE 6 [hp_X]/29.5mL LIQUID PETROLEUM 6 [hp_X]/29.5mL CLOSTRIDIUM BOTULINUM 12 [hp_X]/29.5mL LACHESIS MUTA VENOM 12 [hp_X]/29.5mL SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI 12 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 R207 2026-01-09 R207 2024-01-30 R207 2024-01-30 R207
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9207-1 Argentum Combination9207 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 63083-9207 ARGENTUM COMBINATION 9207 (ARGENTUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_d1870494-1654-42d1-a867-6fd2fe0bfdac.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 63083-9207-1 63083920701 29.5 mL in 1 BOTTLE, DROPPER (63083-9207-1) 29.5 ml 1985-08-15 0000-00-00 No No Current