Home NDC 17312-032-15 Allergy Eyes Relief
Product NDC 17312-032
Requested package NDC 17312-032-15
11-digit product format 173120032
Labeler code 17312
Product ID 17312-032_e4c3c8b0-eb27-8a9c-e053-2995a90a6db1
Type HUMAN OTC DRUG
Nonproprietary name Allium cepa, Ambrosia, Apis, Euphrasia, Histamine hydrochloricum, Sabadilla, Sulphur
Dosage form LIQUID
Route OPHTHALMIC
Labeler TRP Company
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-08-03
Marketing end 0000-00-00
Substance ALLIUM CEPA WHOLE; AMBROSIA ARTEMISIIFOLIA; APIS MELLIFERA; EUPHRASIA STRICTA; HISTAMINE; SCHOENOCAULON OFFICINALE SEED; SULFUR
Active strength 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
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 17312-032 ALLERGY EYES RELIEF (ALLIUM CEPA, AMBROSIA, APIS, EUPHRASIA, HISTAMINE HYDROCHLORICUM, SABADILLA, SULPHUR) LIQUID [TRP COMPANY] 8 Legacy NDC 20230211_58f442e6-c9f5-3b26-e053-2a91aa0ae972.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 17312-032-15 17312003215 1 BOTTLE, DROPPER in 1 PACKAGE (17312-032-15) > 10 mL in 1 BOTTLE, DROPPER 2017-08-03 0000-00-00 No No Current