Home NDC 63083-9303-1 Glyoxal Combination
Product NDC 63083-9303
Requested package NDC 63083-9303-1
11-digit product format 630839303
Labeler code 63083
Product ID 63083-9303_8ca9711d-9513-456b-9b96-6512011755ab
Type HUMAN OTC DRUG
Nonproprietary name Glyoxal Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance (4-METHOXYPHENYL)GLYOXAL; CHELIDONIUM MAJUS WHOLE; DIMETHYL PHTHALATE; FORMALDEHYDE SOLUTION; GELSEMIUM SEMPERVIRENS ROOT; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; SULFUR
Active strength 12; 10; 12; 12; 3; 3; 6; 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
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 Glyoxal Combination
Brand name suffix 9303
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/29.5mL SODIUM CARBONATE 10 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/29.5mL CHELIDONIUM MAJUS WHOLE 12 [hp_X]/29.5mL DIMETHYL PHTHALATE 3 [hp_X]/29.5mL FORMALDEHYDE SOLUTION 3 [hp_X]/29.5mL (4-METHOXYPHENYL)GLYOXAL 6 [hp_X]/29.5mL SULFUR 12 [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 R303 2026-01-09 R303 2024-01-30 R303 2024-01-30 R303
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9303-1 Glyoxal Combination9303 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 63083-9303 GLYOXAL COMBINATION 9303 (GLYOXAL COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_b392b61f-9bfb-4296-b99d-41f1101d26e5.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 63083-9303-1 63083930301 29.5 mL in 1 BOTTLE, DROPPER (63083-9303-1) 29.5 ml 1985-08-15 0000-00-00 No No Current