Home NDC 17312-169-15 Eye Lid Relief
Product NDC 17312-169
Requested package NDC 17312-169-15
11-digit product format 173120169
Labeler code 17312
Product ID 17312-169_f1ed7811-cdc8-23f4-e053-2a95a90af36b
Type HUMAN OTC DRUG
Nonproprietary name EPINEPHRINE, SILVER, CALCIUM SULFATE ANHYDROUS, CLEMATIS RECTA, EUPHRASIA STRICTA, GRAPHITE, GOLDENSEAL
Dosage form LIQUID
Route OPHTHALMIC
Labeler TRP Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-01-11
Marketing end 0000-00-00
Substance CALCIUM SULFATE ANHYDROUS; CLEMATIS RECTA FLOWERING TOP; EPINEPHRINE; EUPHRASIA STRICTA; GOLDENSEAL; GRAPHITE; SILVER
Active strength 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Blood Coagulation Factor [EPC], Calcium [CS], Catecholamine [EPC], Catecholamines [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2024-12-31
Current FDA listing Historical FDA.report record 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 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 I Inactivated by FDA 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 17312-169 EYE LID RELIEF (EPINEPHRINE, SILVER, CALCIUM SULFATE ANHYDROUS, CLEMATIS RECTA, EUPHRASIA STRICTA, GRAPHITE, GOLDENSEAL) LIQUID [TRP COMPANY] 6 Legacy NDC 20230806_c54b3986-2dc1-b42e-e053-2995a90a274b.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 17312-169-15 17312016915 1 BOTTLE, DROPPER in 1 PACKAGE (17312-169-15) > 10 mL in 1 BOTTLE, DROPPER 2021-01-11 0000-00-00 No No Current