b92d959d-dd35-b2a3-e053-2995a90af3ff

SPL v3

SPL

SPL Set ID b92d959d-dd35-b2a3-e053-2995a90af3ff

Route

oral

Published

Effective Date 2021-04-15

Document Type 34390-5 Human OTC Drug Label

Drug Facts

Composition & Product

Active Ingredients

cetirizine (10 mg)

Inactive Ingredients

silicon dioxide croscarmellose sodium hypromellose 2910 (5 mpa.s) lactose monohydrate magnesium stearate microcrystalline cellulose polyethylene glycol 400 titanium dioxide

Identifiers & Packaging

Pill Appearance

Imprint: X;36 Shape: round Color: white Size: 8 mm Score: 1

Marketing Status

anda active Since 2021-03-15

Purpose

Antihistamine

Description

Drug Facts

Medication Information

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Active Ingredient

Cetirizine hydrochloride USP 10 mg

Uses

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

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

Purpose

Antihistamine

Directions

adults and children 6 years and over	one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and over	ask a doctor
children under 6 years of age	ask a doctor
consumers with liver or kidney disease	ask a doctor

Other Information

store between 20° to 25°C (68° to 77°F)
TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.

Inactive Ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.

Description

Drug Facts

Questions?

1-800-632-6900

DISTRIBUTED BY

THE KROGER CO.

CINCINNATI,

OHIO 45202

MADE IN INDIA

Code: TS/DRUGS/19/1993

Section 42229-5

Drug Facts

When Using This Product

drowsiness may occur
avoid alcoholic drinks
alcohol, sedatives, and tranquilizers may increase drowsiness
be careful when driving a motor vehicle or operating machinery

Stop Use and Ask A Doctor If

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

If Pregnant Or Breast Feeding:

If breast-feeding: not recommended
if pregnant: 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]

Ask A Doctor Before Use If You Have

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

Ask A Doctor Or Pharmacist Before Use If You Are

taking tranquilizers or sedatives.

Package Label Principal Display Panel 10 Mg (30's Tablet Container label)

NDC 30142-172-09

KROGER^®

ORIGINAL

PRESCRIPTION STRENGTH

ALLERGY

Cetirizine

Hydrochloride

Tablets USP 10 mg

Antihistamine

24

HOUR

30 TABLETS

10 mg each

Package Label Principal Display Panel 10 Mg (30's Tablet Container Carton Label)

COMPARE TO the active ingredient of ZYRTEC^® ^*See side panel

KROGER^® NDC 30142-172-09

ORIGINAL PRESCRIPTION STRENGTH

ALLERGY

Cetirizine Hydrochloride

Tablets USP 10 mg

Antihistamine

INDOOR & OUTDOOR

ALLERGIES

actual

size

24

HOUR

RELIEF OF:

Sneezing;

Runny Nose;

Itchy, Watery Eyes;

Itchy Throat or Nose

30 TABLETS

10 mg each

Structured Label Content

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Active Ingredient (Active ingredient (in each tablet))

Cetirizine hydrochloride USP 10 mg

Uses

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

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

Purpose

Antihistamine

Directions

adults and children 6 years and over	one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and over	ask a doctor
children under 6 years of age	ask a doctor
consumers with liver or kidney disease	ask a doctor

Other Information (Other information)

store between 20° to 25°C (68° to 77°F)
TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.

Inactive Ingredients (Inactive ingredients)

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.

Questions?

1-800-632-6900

DISTRIBUTED BY

THE KROGER CO.

CINCINNATI,

OHIO 45202

MADE IN INDIA

Code: TS/DRUGS/19/1993

Section 42229-5 (42229-5)

Drug Facts

When Using This Product (When using this product)

drowsiness may occur
avoid alcoholic drinks
alcohol, sedatives, and tranquilizers may increase drowsiness
be careful when driving a motor vehicle or operating machinery

Stop Use and Ask A Doctor If (Stop use and ask a doctor if)

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

If Pregnant Or Breast Feeding: (If pregnant or breast-feeding:)

If breast-feeding: not recommended
if pregnant: ask a health professional before use.

Keep Out of Reach of Children. (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]

Ask A Doctor Before Use If You Have (Ask a doctor before use if you have)

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

Ask A Doctor Or Pharmacist Before Use If You Are (Ask a doctor or pharmacist before use if you are)

taking tranquilizers or sedatives.

Package Label Principal Display Panel 10 Mg (30's Tablet Container label) (PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30's Tablet Container Label))

NDC 30142-172-09

KROGER^®

ORIGINAL

PRESCRIPTION STRENGTH

ALLERGY

Cetirizine

Hydrochloride

Tablets USP 10 mg

Antihistamine

24

HOUR

30 TABLETS

10 mg each

Package Label Principal Display Panel 10 Mg (30's Tablet Container Carton Label) (PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30's Tablet Container Carton Label))

Sneezing;

Runny Nose;

Itchy, Watery Eyes;

Itchy Throat or Nose

30 TABLETS

10 mg each

Advanced Ingredient Data

[{"name": "CETIRIZINE", "unii": "YO7261ME24", "classCode": "ACTIB", "strengthNumerator": "10", "strengthDenominator": "1", "strengthNumeratorUnit": "mg", "strengthDenominatorUnit": "1"}, {"name": "SILICON DIOXIDE", "unii": "ETJ7Z6XBU4", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "CROSCARMELLOSE SODIUM", "unii": "M28OL1HH48", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "HYPROMELLOSE 2910 (5 MPA.S)", "unii": "R75537T0T4", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "LACTOSE MONOHYDRATE", "unii": "EWQ57Q8I5X", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "MAGNESIUM STEARATE", "unii": "70097M6I30", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "MICROCRYSTALLINE CELLULOSE", "unii": "OP1R32D61U", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "POLYETHYLENE GLYCOL 400", "unii": "B697894SGQ", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}, {"name": "TITANIUM DIOXIDE", "unii": "15FIX9V2JP", "classCode": "IACT", "strengthNumerator": "", "strengthDenominator": "", "strengthNumeratorUnit": "", "strengthDenominatorUnit": ""}]

Raw Label Data

All Sections (JSON)

{"Uses": "temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat", "42229-5": "Drug Facts", "Purpose": "Antihistamine", "Warnings": "Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.", "Directions": "adults and children 6 years and over one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. adults 65 years and over ask a doctor children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor", "Questions?": "1-800-632-6900 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 MADE IN INDIA Code: TS/DRUGS/19/1993", "Other information": "store between 20° to 25°C (68° to 77°F) TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.", "Inactive ingredients": "colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.", "When using this product": "drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery", "Stop use and ask a doctor if": "an allergic reaction to this product occurs. Seek medical help right away.", "If pregnant or breast-feeding:": "If breast-feeding: not recommended if pregnant: 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]", "Active ingredient (in each tablet)": "Cetirizine hydrochloride USP 10 mg", "Ask a doctor before use if you have": "liver or kidney disease. Your doctor should determine if you need a different dose.", "Ask a doctor or pharmacist before use if you are": "taking tranquilizers or sedatives.", "PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30's Tablet Container Label)": "NDC 30142-172-09 KROGER ® ORIGINAL PRESCRIPTION STRENGTH ALLERGY Cetirizine Hydrochloride Tablets USP 10 mg Antihistamine 24 HOUR 30 TABLETS 10 mg each", "PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30's Tablet Container Carton Label)": "COMPARE TO the active ingredient of ZYRTEC ® * See side panel KROGER ® NDC 30142-172-09 ORIGINAL PRESCRIPTION STRENGTH ALLERGY Cetirizine Hydrochloride Tablets USP 10 mg Antihistamine INDOOR & OUTDOOR ALLERGIES actual size 24 HOUR RELIEF OF: Sneezing; Runny Nose; Itchy, Watery Eyes; Itchy Throat or Nose 30 TABLETS 10 mg each"}

Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:59:31.388374 · Updated: 2026-03-14T22:59:31.191887