Home NDC 63083-9255-1 Euphorbium Combination
Product NDC 63083-9255
Requested package NDC 63083-9255-1
11-digit product format 630839255
Labeler code 63083
Product ID 63083-9255_8f5de206-b87d-4fdb-bb58-292b0afb7b59
Type HUMAN OTC DRUG
Nonproprietary name Euphorbium Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance PLANTAGO MAJOR WHOLE; PULSATILLA MONTANA WHOLE; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; SUS SCROFA NASAL MUCOSA; SILVER NITRATE; CALCIUM SULFIDE; SINUSITISINUM; DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN
Active strength 3; 4; 6; 6; 8; 8; 10; 10; 12; 30 [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 Euphorbium Combination
Brand name suffix 9255
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PLANTAGO MAJOR WHOLE 3 [hp_X]/29.5mL PULSATILLA MONTANA WHOLE 4 [hp_X]/29.5mL EUPHORBIA RESINIFERA RESIN 6 [hp_X]/29.5mL LUFFA OPERCULATA FRUIT 6 [hp_X]/29.5mL MERCURIC IODIDE 8 [hp_X]/29.5mL SUS SCROFA NASAL MUCOSA 8 [hp_X]/29.5mL SILVER NITRATE 10 [hp_X]/29.5mL CALCIUM SULFIDE 10 [hp_X]/29.5mL SINUSITISINUM 12 [hp_X]/29.5mL DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN 30 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 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 R255 2026-01-09 R255 2024-01-30 R255 2024-01-30 R255
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9255-1 Euphorbium Combination9255 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 63083-9255 EUPHORBIUM COMBINATION 9255 (EUPHORBIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_ff642588-439e-4e79-8c7b-3d388938eca5.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 63083-9255-1 63083925501 29.5 mL in 1 BOTTLE, DROPPER (63083-9255-1) 29.5 ml 1985-08-15 0000-00-00 No No Current