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NDC 00363-0752-30 Loratadine 5 mg/1 Details
Loratadine 5 mg/1
Loratadine is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by WALGREEN COMPANY. The primary component is LORATADINE.
MedlinePlus Drug Summary
Loratadine is used to temporarily relieve the symptoms of hay fever (allergy to pollen, dust, or other substances in the air) and other allergies. These symptoms include sneezing, runny nose, and itchy eyes, nose, or throat. Loratadine is also used to treat itching and redness caused by hives. However, loratadine does not prevent hives or other allergic skin reactions. Loratadine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms. Loratadine is also available in combination with pseudoephedrine (Sudafed, others). This monograph only includes information about the use of loratadine alone. If you are taking the loratadine and pseudoephedrine combination product, read the information on the package label or ask your doctor or pharmacist for more information.
Related Packages: 00363-0752-30Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
NDC | 00363-0752 |
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Product ID | 0363-0752_67ced469-3068-49b4-988b-ac440ee968a4 |
Associated GPIs | |
GCN Sequence Number | 062450 |
GCN Sequence Number Description | chlorpheniramine/dextromethorp LIQUID 2-15 MG/15 ORAL |
HIC3 | B4E |
HIC3 Description | NON-OPIOID ANTITUSSIVE-1ST GEN ANTIHISTAMINE COMB. |
GCN | 98226 |
HICL Sequence Number | 001924 |
HICL Sequence Number Description | CHLORPHENIRAMINE MALEATE/DEXTROMETHORPHAN HBR |
Brand/Generic | Generic |
Proprietary Name | Loratadine |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Loratadine |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, CHEWABLE |
Route | ORAL |
Active Ingredient Strength | 5 |
Active Ingredient Units | mg/1 |
Substance Name | LORATADINE |
Labeler Name | WALGREEN COMPANY |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA210088 |
Listing Certified Through | 2024-12-31 |
Package
Package Images

NDC 00363-0752-30 (00363075230)
NDC Package Code | 0363-0752-30 |
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Billing NDC | 00363075230 |
Package | 3 BLISTER PACK in 1 CARTON (0363-0752-30) / 10 TABLET, CHEWABLE in 1 BLISTER PACK |
Marketing Start Date | 2019-07-26 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 645c26ab-08ab-4a69-ae7d-7802d8ec5922 Details
Uses
Warnings
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
Directions
- chew or crush tablets completely before swallowing.
adults and children 6 years and over | chew 2 tablets daily; not more than 2 tablets in 24 hours |
children 2 to under 6 years of age | chew 1 tablet daily; not more than 1 tablet in 24 hours |
children under 2 years of age | ask a doctor |
consumers with liver or kidney disease | ask a doctor |
Other information
Inactive ingredients
PRINCIPAL DISPLAY PANEL - 30 Tablet Blister Pack Carton
Walgreens
children's
ALLERGY
Wal-itin®
LORATADINE CHEWABLE TABLETS USP, 5 mg / ANTIHISTAMINE
Compare to Children's Claritin®
Chewables active ingredient††
NDC 0363-0752-30
NEW
CHEWABLE
NON-DROWSY*
24-HOUR RELIEF
- 24-hour relief of sneezing, runny nose,
itchy throat or nose, & itchy, watery eyes - Indoor & outdoor allergies
30 CHEWABLE
TABLETS
The chewable tablets are to be chewed before swallowing.
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
GRAPE
FLAVOR
ACTUAL SIZE
AGES
2
YEARS &
OLDER

INGREDIENTS AND APPEARANCE
LORATADINE
loratadine tablet, chewable |
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Labeler - WALGREEN COMPANY (008965063) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Ohm Laboratories Inc. | 184769029 | MANUFACTURE(0363-0752) |