up and up allergy relief

Product NDC: 11673-612
Requested package NDC: 11673-612-58
11-digit product format: 116730612
Labeler code: 11673
Product ID: 11673-612_244b9b86-cddc-46fb-8f03-312a3fed96d1
Type: HUMAN OTC DRUG
Nonproprietary name: Loratadine
Dosage form: TABLET
Route: ORAL
Labeler: Target Corporation
Application: ANDA076301
Marketing category: ANDA
Marketing start: 2012-03-26
Substance: LORATADINE
Active strength: 10 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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	11673-612	11673-612-58	D	Discontinued by firm		2026-08-17

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-612	11673-612-58	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	11673-612	11673-612-58	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 42.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A076301-001	LORATADINE	LORATADINE	10MG	TABLET / ORAL			2004-06-25

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 42 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-08-18 06:07:40	2026-07	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A076301-001	LORATADINE	10MG	TABLET / ORAL	2004-06-25	`e64feba35796…`

Additional Listing Data#

Finished product: Yes
Brand name base: up and up allergy relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LORATADINE	10 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
7AJO3BO7QN	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
311372	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c4ef0110-89c3-4ded-9a9a-75c0f794f869	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11673-612-03	up and up allergy relief	70 in 1 BOTTLE	TABLET	70	10
11673-612-03	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-46	up and up allergy relief	1 in 1 BLISTER PACK	TABLET	1	10
11673-612-46	up and up allergy relief	10 in 1 CARTON	TABLET	10	10
11673-612-58	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-58	up and up allergy relief	40 in 1 BOTTLE	TABLET	40	10
11673-612-65	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-65	up and up allergy relief	30 in 1 BOTTLE	TABLET	30	10
11673-612-72	up and up allergy relief	60 in 1 BOTTLE	TABLET	60	10
11673-612-72	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-76	up and up allergy relief	120 in 1 BOTTLE	TABLET	120	10
11673-612-76	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-78	up and up allergy relief	100 in 1 BOTTLE	TABLET	100	10
11673-612-82	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-82	up and up allergy relief	200 in 1 BOTTLE	TABLET	200	10
11673-612-87	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-87	up and up allergy relief	300 in 1 BOTTLE	TABLET	300	10
11673-612-95	up and up allergy relief	1 in 1 CARTON	TABLET	1	10
11673-612-95	up and up allergy relief	45 in 1 BOTTLE	TABLET	45	10

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
11673-612-46	EA - Each	11673-612	19931e59-7a9d-49bb-9c62-3adfc07178ac	1	2015-07-20
11673-612-82	EA - Each	11673-612	31370ba1-9f78-4630-bf95-d79ce5d368e2	1	2015-07-20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
LORATADINE	ACTIVE INGREDIENT	7AJO3BO7QN	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	5
LORATADINE	ACTIVE MOIETY	7AJO3BO7QN	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	5
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	5
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	5
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-612	UP AND UP ALLERGY RELIEF (LORATADINE) TABLET [TARGET CORPORATION]	9	Current NDC, Legacy NDC, 19 package rows	20250331_c4ef0110-89c3-4ded-9a9a-75c0f794f869.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 3 · 43 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
allergy relief	LORATADINE	Walgreen Company	41f8fc1d-2d14-48da-a233-23e9c11296d9	2026-07-23	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
dg health allergy relief	LORATADINE	Dolgencorp Inc	dfc4b065-1980-48ec-9c3e-aaa4a42214d3	2026-07-02	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
CareOne Allergy Relief 24 Hour	LORATADINE	American Sales Company	bbd5424f-fa5b-4955-8542-7011b19400ea	2026-07-01	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
allergy relief	LORATADINE	Rite Aid Corporation	5d58ed7a-e40b-417f-a216-5ec6721d361b	2026-05-27	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
good sense allergy relief	LORATADINE	L. Perrigo Company	80e8a6e8-0c5f-4065-9545-112e146d25ee	2026-04-27	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine antihistamine	LORATADINE	PD-Rx Pharmaceuticals, Inc.	039f144b-891b-4ab0-e063-6394a90aa4c8	2026-02-26	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine antihistamine	LORATADINE	PD-Rx Pharmaceuticals, Inc.	775885f9-0580-4eca-94d8-44fce1dcdccd	2026-02-26	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
allergy relief	LORATADINE	CVS Pharmacy	0038bc38-c205-4d8d-ab78-1abbcd76829e	2026-02-25	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Berkley and Jensen Allergy Relief	LORATADINE	BJWC	e981a0ef-08e9-4ac3-92a1-411217e0a251	2026-02-16	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine	LORATADINE	Major Pharmaceuticals	60162446-4fa1-4ee3-ae20-19fadc2491ab	2026-02-09	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Allergy Relief	LORATADINE	Kroger Company	dac0b200-6b02-4c8a-b1dd-a4d5341dfb2d	2026-02-05	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Allergy Relief	LORATADINE	HyVee Inc	b6ee2b7f-8e01-4962-b28f-91e5cac85276	2026-01-28	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine antihistamine	LORATADINE	NCS HealthCare of KY, LLC dba Vangard Labs	f3d05276-21bd-419d-8dba-07ce278d3375	2025-12-22	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine	LORATADINE	Major Pharmaceuticals	dee25423-377b-4b94-a4a8-0dfb8f51aaab	2025-12-08	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine antihistamine	LORATADINE	A-S Medication Solutions	1203981a-becd-4854-810d-b6d8842b5bd2	2025-12-06	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
goodnow allergy relief	LORATADINE	Gobrands, Inc	352a1268-7f44-417d-a46a-f0cc2e944a26	2025-11-15	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine	LORATADINE	A-S Medication Solutions	0eade963-be64-4718-a370-7e78efb91fc4	2025-11-06	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine	LORATADINE	A-S Medication Solutions	6f82e0ab-2c01-4afb-8d0f-b0c06819d1b0	2025-11-06	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine	LORATADINE	A-S Medication Solutions	4cee60b6-b32b-47d0-aa00-a7ea1a7ed3cf	2025-11-06	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301
Loratadine antihistamine	LORATADINE	Padagis Israel Pharmaceuticals Ltd	c72d8a30-520e-4d25-8f02-0c891e070a1a	2025-09-12	Warnings	Exact identifier application applno (ANDA): 076301 application number: ANDA076301

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7AJO3BO7QN	LORATADINE	79794-75-5	LORATADINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
311372	loratadine 10 MG 24HR Oral Tablet	PSN	c4ef0110-89c3-4ded-9a9a-75c0f794f869	10
311372	loratadine 10 MG Oral Tablet	SCD	c4ef0110-89c3-4ded-9a9a-75c0f794f869	10
311372	loratadine 10 MG 24 HR Oral Tablet	SY	c4ef0110-89c3-4ded-9a9a-75c0f794f869	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-612-58	11673061258	1 BOTTLE in 1 CARTON (11673-612-58) > 40 TABLET in 1 BOTTLE	1 bottle	2015-03-25	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	2025-03-28	HUMAN OTC DRUG LABEL	10