Allergy Eyes Day and Night Relief Pack

Product NDC: 17312-182
Requested package NDC: 17312-182-20
11-digit product format: 173120182
Labeler code: 17312
Product ID: 17312-182_cbab48dd-efaa-f04e-e053-2a95a90a9c35
Type: HUMAN OTC DRUG
Nonproprietary name: Allium cepa, Ambrosia, Apis, Euphrasia, Histamine hydrochloricum, Sabadilla, Sulphur
Dosage form: KIT
Labeler: TRP Company
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2020-04-11
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	17312-182	17312-182-20	D	Discontinued by firm		2026-10-05

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 · 9 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	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
17312-182-20	2025-11-17	C162847	48780-1	2cef2736-6cc9-d83d-e063-dadaa90ab31f	Allergy Eyes Day & Night Relief Pack
17312-182-20	2025-01-30	C162847	48780-1	2cef2736-6cc9-d83d-e063-dadaa90ab31f	Allergy Eyes Day & Night Relief Pack

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17312-182	ALLERGY EYES DAY AND NIGHT RELIEF PACK DAY AND NIGHT RELIEF PACK (ALLIUM CEPA, AMBROSIA, APIS, EUPHRASIA, HISTAMINE HYDROCHLORICUM, SABADILLA, SULPHUR) KIT [TRP COMPANY]	2	Legacy NDC	20210912_a343cc01-46ae-13ab-e053-2a95a90a50c1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17312-182-20	17312018220	1 KIT in 1 CARTON (17312-182-20) * 10 mL in 1 BOTTLE * 4 g in 1 TUBE	1 kit	2020-04-11	0000-00-00	No	No	Current