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NDC 63868-0462-30 Allergy Relief 10 mg/1 Details
Allergy Relief 10 mg/1
Allergy Relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by QUALITY CHOICE (Chain Drug Marketing Association). 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: 63868-0462-30Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
| NDC | 63868-0462 |
|---|---|
| Product ID | 63868-462_847b0a98-4af6-45a3-aead-f499125080a8 |
| 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 | Allergy Relief |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Loratadine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | LORATADINE |
| Labeler Name | QUALITY CHOICE (Chain Drug Marketing Association) |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075209 |
| Listing Certified Through | n/a |
Package
Package Images
NDC 63868-0462-30 (63868046230)
| NDC Package Code | 63868-462-30 |
|---|---|
| Billing NDC | 63868046230 |
| Package | 1 BOTTLE, PLASTIC in 1 BOX (63868-462-30) / 30 TABLET in 1 BOTTLE, PLASTIC |
| Marketing Start Date | 2019-02-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL e099ccd5-61b1-49ad-8cf7-677d93b6e18a 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
Inactive ingredients
Principal Display Panel
†Compare to the Active Ingredient in Claritin®
Original Prescription Strength
Allergy Relief
Loratadine Tablets, USP
10 mg | Antihistamine
Indoor & Outdoor Allergies
Relief of:
Sneezing | Runny Nose
Itchy, Watery Eyes | Itchy Throat or Nose
Gluten Free
24 Hour Allergy Relief | Non-Drowsy*
Tablets
*When taken as directed. See Drug Facts panel.
†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin®.
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW ANY SIGN OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
Distributed by C.D.M.A., Inc.©
43157 W 9 Mile Rd
Novi, MI 48375
INGREDIENTS AND APPEARANCE
| ALLERGY RELIEF
loratadine tablet |
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| Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774) |