Home NDC 63083-2074-2 Glaucoma Drops
Product NDC 63083-2074
Requested package NDC 63083-2074-2
11-digit product format 630832074
Labeler code 63083
Product ID 63083-2074_617f1878-a655-425b-a81f-a979be629a44
Type HUMAN OTC DRUG
Nonproprietary name Glaucoma Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance PLECTRANTHUS BARBATUS ROOT OIL; BILBERRY; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; SPIGELIA ANTHELMIA WHOLE; GOLDENSEAL; ACONITUM NAPELLUS WHOLE; AMARYLLIS BELLADONNA WHOLE; BOS TAURUS EYE; BRYONIA ALBA ROOT; PHOSPHORUS
Active strength 2; 2; 3; 3; 3; 5; 6; 6; 6; 12; 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
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 Glaucoma Drops
Brand name suffix 2074
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PLECTRANTHUS BARBATUS ROOT OIL 2 [hp_X]/59mL BILBERRY 2 [hp_X]/59mL EUPHRASIA STRICTA 3 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT 3 [hp_X]/59mL SPIGELIA ANTHELMIA WHOLE 3 [hp_X]/59mL GOLDENSEAL 5 [hp_X]/59mL ACONITUM NAPELLUS WHOLE 6 [hp_X]/59mL AMARYLLIS BELLADONNA WHOLE 6 [hp_X]/59mL BOS TAURUS EYE 6 [hp_X]/59mL BRYONIA ALBA ROOT 12 [hp_X]/59mL PHOSPHORUS 12 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 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 C74 2026-01-09 C74 2024-01-30 C74 2024-01-30 C74
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2074-2 Glaucoma Drops2074 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 63083-2074 GLAUCOMA DROPS 2074 (GLAUCOMA DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_7cf2052e-15f8-4b04-ae18-1847da8f4236.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 63083-2074-2 63083207402 59 mL in 1 BOTTLE, DROPPER (63083-2074-2) 59 ml 1985-08-15 0000-00-00 No No Current