Home NDC 63083-6014-2 Opsin I
Product NDC 63083-6014
Requested package NDC 63083-6014-2
11-digit product format 630836014
Labeler code 63083
Product ID 63083-6014_bca11e36-d24b-43e5-bded-e202480df00f
Type HUMAN OTC DRUG
Nonproprietary name Opsin I
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ACETALDEHYDE; ACTIVATED CHARCOAL; ARSENIC TRIOXIDE; COUMARIN; DEOXYMUTAASPERGILLIC ACID; EPINEPHRINE; GALLIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; HYDRANGEA ARBORESCENS ROOT; INDOLE-3-CARBINOL; LIQUID PETROLEUM; RUTIN; SILVER NITRATE; YEAST MANNAN
Active strength 12; 6; 6; 12; 30; 6; 12; 12; 6; 12; 6; 12; 6; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [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…
Additional Listing Data#
Finished product Yes
Brand name base Opsin I
Brand name suffix 6014
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength EPINEPHRINE 12 [hp_X]/59mL SILVER NITRATE 6 [hp_X]/59mL ARSENIC TRIOXIDE 6 [hp_X]/59mL ACTIVATED CHARCOAL 12 [hp_X]/59mL HYDRANGEA ARBORESCENS ROOT 30 [hp_X]/59mL LIQUID PETROLEUM 6 [hp_X]/59mL ACETALDEHYDE 12 [hp_X]/59mL COUMARIN 12 [hp_X]/59mL GALLIC ACID MONOHYDRATE 6 [hp_X]/59mL HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/59mL INDOLE-3-CARBINOL 6 [hp_X]/59mL YEAST MANNAN 12 [hp_X]/59mL RUTIN 6 [hp_X]/59mL DEOXYMUTAASPERGILLIC ACID 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 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 X14 2026-01-09 X14 2024-01-30 X14 2024-01-30 X14
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-6014-2 Opsin I6014 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-6014 OPSIN I 6014 (OPSIN I) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220406_ac4185b4-7b9b-4608-9157-d8be86582ff8.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 63083-6014-2 63083601402 59 mL in 1 BOTTLE, DROPPER (63083-6014-2) 59 ml 1985-08-15 0000-00-00 No No Current