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NDC 30142-0996-30 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 KROGER 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: 30142-0996-30Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
| NDC | 30142-0996 |
|---|---|
| Product ID | 30142-996_6f7f7005-22db-4b88-9771-e31c21e9b2b1 |
| 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 | 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 | KROGER 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 30142-0996-30 (30142099630)
| NDC Package Code | 30142-996-30 |
|---|---|
| Billing NDC | 30142099630 |
| Package | 3 BLISTER PACK in 1 CARTON (30142-996-30) / 10 TABLET, CHEWABLE in 1 BLISTER PACK |
| Marketing Start Date | 2019-05-22 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 6f7f7005-22db-4b88-9771-e31c21e9b2b1 Details
Uses
Warnings
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Ask a doctorbefore 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.
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.
Directions
Other information
Inactive ingredients
Questions?
Principal Display Panel – 30 Chewable Tablet Blister Pack Carton
NDC 30142-996-30
†Compare to the active ingredient of Children’s Claritin® Chewables
ages 2 years and older
Non-Drowsy
Children’s Allergy Relief
Loratadine Chewable Tablets USP, 5 mg
Antihistamine
Indoor & Outdoor Allergies
30 CHEWABLE TABLETS
The chewable tablets are to be chewed before swallowing.
Grape Flavored
24 Hour Relief Of:
- •
- Sneezing
- •
- Runny Nose
- •
- Itchy, Watery Eyes
- •
- Itchy Nose or Throat
*When taken as directed. See Drug Facts Panel.
INGREDIENTS AND APPEARANCE
| LORATADINE
loratadine tablet, chewable |
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| Labeler - KROGER COMPANY (006999528) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| Ohm Laboratories Inc. | 184769029 | MANUFACTURE(30142-996) | |