up and up allergy relief

Product NDC: 11673-462
11-digit product format: 116730462
Labeler code: 11673
Product ID: 11673-462_e5d553df-3a06-4b9d-ba49-c5222d55f69f
Type: HUMAN OTC DRUG
Nonproprietary name: diphenhydramine hydrochloride
Dosage form: CAPSULE
Route: ORAL
Labeler: Target Corporation
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2009-06-10
Marketing end: 0000-00-00
Substance: DIPHENHYDRAMINE HYDROCHLORIDE
Active strength: 25 mg/1
NDC exclude flag: No
Listing certified through: 2020-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	11673-462		D	Discontinued by firm	2026-10-16
excluded package	package	11673-462	11673-462-62	D	Discontinued by firm	2026-10-16
excluded package	package	11673-462	11673-462-78	D	Discontinued by firm	2026-10-16

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 · 34 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-462-62	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-462-78	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-462-62	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-462-78	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11673-462-62	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	11673-462-78	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11673-462-62	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	11673-462-78	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11673-462-62	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	11673-462-78	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11673-462-62	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	11673-462-78	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11673-462-62	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	11673-462-78	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11673-462-62	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	11673-462-78	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11673-462-62	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	11673-462-78	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	11673-462-62	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	11673-462-78	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	11673-462-62	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	11673-462-78	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	11673-462-62	`557ba5c1ecfa…`	`9c80585c8c6e…`

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
11673-462-62	2024-01-30	C162847	48780-1	1030e365-6651-111a-e063-dadaa90a10e2	Target Corporation Allergy Relief Drug Facts
11673-462-78	2024-01-30	C162847	48780-1	1030e365-6651-111a-e063-dadaa90a10e2	Target Corporation Allergy Relief Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
11673-462-62	EA - Each	11673-462	20ab16e2-77b2-44ba-b957-ef0ef81ccef3	1	2012-07-24
11673-462-78	EA - Each	11673-462	784a761a-c48c-4a99-9c89-30545618ba31	1	2015-07-20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
ANHYDROUS LACTOSE	INACTIVE INGREDIENT	3SY5LH9PMK	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
D&C RED NO. 28	INACTIVE INGREDIENT	767IP0Y5NH	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
EDETATE CALCIUM DISODIUM	INACTIVE INGREDIENT	25IH6R4SGF	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
GELATIN	INACTIVE INGREDIENT	2G86QN327L	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3
SODIUM PROPIONATE	INACTIVE INGREDIENT	DK6Y9P42IN	UP AND UP ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE [TARGET CORPORATION]	3

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
TC2D6JAD40	DIPHENHYDRAMINE HYDROCHLORIDE	147-24-0	DIPHENHYDRAMINE HYDROCHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-462-78	11673046278	1 BOTTLE in 1 CARTON (11673-462-78) > 100 CAPSULE in 1 BOTTLE	1 bottle	2009-09-16	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Target Corporation Allergy Relief Drug Facts	Target Corporation	2017-01-19	HUMAN OTC DRUG LABEL	4