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NDC 36800-0691-95 topcare allergy relief 180 mg/1 Details

topcare allergy relief 180 mg/1

topcare allergy relief is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Topco Associates LLC. The primary component is FEXOFENADINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms.

Related Packages: 36800-0691-95
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Fexofenadine

Product Information

NDC	36800-0691
Product ID	36800-691_51cf462b-21b6-44e2-b97a-da14622f3947
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	topcare allergy relief
Proprietary Name Suffix	n/a
Non-Proprietary Name	fexofenadine hydrochloride
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	180
Active Ingredient Units	mg/1
Substance Name	FEXOFENADINE HYDROCHLORIDE
Labeler Name	Topco Associates LLC
Pharmaceutical Class	Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA212971
Listing Certified Through	2024-12-31

Package

Package Images

NDC 36800-0691-95 (36800069195)

Pricing Information	N/A
NDC Package Code	36800-691-95
Billing NDC	36800069195
Package	1 BOTTLE in 1 CARTON (36800-691-95) / 45 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date	2021-09-21
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL e7658b5f-2d78-4f25-b1a3-e49198ca8f32 Details

Active ingredient (in each tablet)

Fexofenadine HCl 180 mg

Purpose

Antihistamine

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

Warnings

Do not use

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

Ask a doctor before use if you have

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

When using this product

•: 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

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

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

•: do not use if printed blister unit is broken or torn
•: store between 20° -25°C (68° -77°F)
•: protect from excessive moisture
•: this product meets the requirements of USP Dissolution Test 2

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, FD&C blue #2 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, talc, titanium dioxide

Questions or comments?

1-888-423-0139

Package/Label Principal Display Panel

COMPARE TO ALLEGRA® ALLERGY ACTIVE INGREDIENT

NON-DROWSY

Allergy Relief

FEXOFENADINE HYDROCHLORIDE TABLETS, 180 mg (ANTIHISTAMINE)

24 HR

INDOOR/OUTDOOR ALLERGY RELIEF

- Sneezing – Runny Nose

- Itchy, Watery Eyes

- Itchy Nose or Throat

5 TABLETS

actual size

INGREDIENTS AND APPEARANCE

TOPCARE ALLERGY RELIEF

fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:36800-691
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	180 mg

Ingredient Name	Strength
Inactive Ingredients
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	PINK	Score	no score
Shape	OVAL	Size	18mm
Flavor		Imprint Code	L847
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:36800-691-13	5 in 1 CARTON	08/27/2021
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:36800-691-39	1 in 1 CARTON	08/23/2021
2		30 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:36800-691-22	15 in 1 CARTON	09/21/2021
3		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC:36800-691-49	1 in 1 CARTON	09/21/2021
4		40 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:36800-691-95	1 in 1 CARTON	09/21/2021
5		45 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC:36800-691-75	1 in 1 CARTON	09/21/2021
6		90 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA212971	08/23/2021

Labeler - Topco Associates LLC (006935977)

Revised: 9/2021

Document Id: 51cf462b-21b6-44e2-b97a-da14622f3947

Set id: e7658b5f-2d78-4f25-b1a3-e49198ca8f32

Version: 2

Effective Time: 20210921