Fexofenadine Hydrochloride

Manufacturer: Northwind Health Company, LLC
Effective date: 2026-01-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:37:06

Label at a glance#

ProductFexofenadine Hydrochloride

Active ingredientFEXOFENADINE HYDROCHLORIDE

Label structure10 sections

Indications and uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Dosage and administration

adults and children 12 years of age and over take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor

Storage and handling

each tablet contain : sodium 8 mg store between 20 to 25°C (68 to 77°F) protect from excessive moisture this product meets the requirements of USP Dissolution Test 2

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-800-616-2471

Label contents#

Full prescribing information#

Active ingredient (in each film-coated tablet)

OTC - ACTIVE INGREDIENT SECTION

Fexofenadine HCL 180 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose
itchy, watery eyes
sneezing
itching of the nose or throat

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease. Your doctor should determine if you need a different dose.

When using this product

OTC - WHEN USING SECTION

do not take more than directed
do not take at the same time as aluminum or magnesium antacids
do not take with fruit juices (see Directions)

Stop use and ask a doctor if

OTC - STOP USE SECTION

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years of age and over	take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of age	do not use
adults 65 years of age and older	ask a doctor
consumers with kidney disease	ask a doctor

Other information

STORAGE AND HANDLING SECTION

each tablet contain: sodium 8 mg
store between 20 to 25°C (68 to 77°F)
protect from excessive moisture
this product meets the requirements of USP Dissolution Test 2

Inactive ingredients

INACTIVE INGREDIENT SECTION

anhydrous lactose, colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, lactose monohydrate, polyethylene glycol, pregelatinized starch (maize), red iron oxide, stearic acid, titanium dioxide, and yellow iron oxide

Questions or comments?

OTC - QUESTIONS SECTION

Call: 1-800-616-2471

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPARE TO the active ingredient in ALLEGRA® ALLERGY 24 HOUR*

FEXOFENADINE HYDROCHLORIDE USP 180 mg

Antihistamine

ALLERGY RELIEF

24-HOUR Relief of:

sneezing
Runny nose
Itchy, watery eyes
Itchy nose or throat

Indoor and Outdoor

Allergy Relief

Non-Drowsy

Capsule Shaped Tablets

*This product is not manufactured or distributed by Chattem Inc., distributor of Allegra® Allergy 24 hour

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Distributed by:

MAJOR® PHARMACEUTICALS

17177 N Laurel Park Drive, Suite 233

Livonia, MI 48152

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 51655-231-52

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
997420	fexofenadine HCl 180 MG 24 HR Oral Tablet	PSN	2
997420	fexofenadine hydrochloride 180 MG Oral Tablet	SCD	2
997420	fexofenadine HCl 180 MG 24 HR Oral Tablet	SY	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
FEXOFENADINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	Data Matrix	(01)00351655231524(21)000000000000000(17)000000(10)0000000000	GTIN-14: 00351655231524 GTIN-12: 351655231524 UPC-A: 351655231524 EAN-13: 0351655231524 GTIN storage (14 digits): 00351655231524	51655-231-52 - Rev B 01-23 NHC.jpg
Data code	Code 128	0000000000		51655-231-52 - Rev B 01-23 NHC.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b893258d-0942-3d8a-3411-056ea0788ff5	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-231-26	2026-01-29	C162847	48780-1	49896155-c57c-586f-e063-e6dba90add90	f2b6c157-1af1-8d43-e053-2995a90aaf1a
51655-231-52	2026-01-29	C162847	48780-1	49896155-c57c-586f-e063-e6dba90add90	f2b6c157-1af1-8d43-e053-2995a90aaf1a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51655-231-26	Fexofenadine Hydrochloride	90 in 1 BOTTLE, PLASTIC	TABLET	90		2
51655-231-52	Fexofenadine Hydrochloride	30 in 1 BOTTLE, PLASTIC	TABLET	30		2

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-7050-40	EA - Each	0904-7050	117e3570-1242-43c4-bd5e-a74ba384b7ab	1	2020-03-10
0904-7050-60	EA - Each	0904-7050	90fd9bed-eb80-4f56-b9fa-d27a4ddcba2c	1	2020-03-10

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Fexofenadine Hydrochloride
Fexofenadine HCl
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
HYPROMELLOSES
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
ANHYDROUS LACTOSE
STARCH, CORN
POLYETHYLENE GLYCOL, UNSPECIFIED
LACTOSE MONOHYDRATE
STEARIC ACID
TITANIUM DIOXIDE
FEXOFENADINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51655-231	51655-231-52, 51655-231-26
0904-7050

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
HYPROMELLOSES	3NXW29V3WO	IACT
FERRIC OXIDE RED	1K09F3G675	IACT
FERRIC OXIDE YELLOW	EX438O2MRT	IACT
ANHYDROUS LACTOSE	3SY5LH9PMK	IACT
STARCH, CORN	O8232NY3SJ	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT
LACTOSE MONOHYDRATE	EWQ57Q8I5X	IACT
STEARIC ACID	4ELV7Z65AP	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
FEXOFENADINE HYDROCHLORIDE	2S068B75ZU	ACTIB

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	Approval date
A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	FEXOFENADINE HYDROCHLORIDE	60MG	TABLET / ORAL	2015-09-16
A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	FEXOFENADINE HYDROCHLORIDE	180MG	TABLET / ORAL	2015-09-16
A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	FEXOFENADINE HYDROCHLORIDE	60MG	TABLET / ORAL	2015-09-16
A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	FEXOFENADINE HYDROCHLORIDE	180MG	TABLET / ORAL	2015-09-16

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 5 · 172 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A204507-002	FEXOFENADINE HYDROCHLORIDE ALLERGY	60MG	TABLET / ORAL	2015-09-16	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A204507-003	FEXOFENADINE HYDROCHLORIDE ALLERGY	180MG	TABLET / ORAL	2015-09-16	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A204507-004	FEXOFENADINE HYDROCHLORIDE HIVES	60MG	TABLET / ORAL	2015-09-16	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A204507-005	FEXOFENADINE HYDROCHLORIDE HIVES	180MG	TABLET / ORAL	2015-09-16	`5bbf6a4d5a75…`

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 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fexofenadine Hydrochloride	FEXOFENADINE HCL	Northwind Health Company, LLC	f2b6c157-1af1-8d43-e053-2995a90aaf1a	2026-01-01	Warnings	Exact identifier ndc (package): 51655-231-52 ndc (package): 51655-231-26 ndc (product): 51655-231 ndc11 (package): 51655023152 ndc11 (package): 51655023126 spl id: 48d2c7f6-8550-1b9c-e063-6394a90ada4e spl set id: f2b6c157-1af1-8d43-e053-2995a90aaf1a
Fexofenadine Hydrochloride	FEXOFENADINE HCL	Major Pharmaceuticals	c34cda59-8a63-48ab-a19d-c06a1878f5da	2025-07-18	Warnings	Exact identifier ndc (product): 0904-7050

Reported adverse events (FAERS/openFDA)#

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