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NDC 11673-0612-82 up and up allergy relief 10 mg/1 Details
up and up allergy relief 10 mg/1
up and up allergy relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. 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: 11673-0612-82Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
| NDC | 11673-0612 |
|---|---|
| Product ID | 11673-612_a136b013-3a10-444a-8a58-36af71f0aa72 |
| Associated GPIs | 41550030000320 |
| GCN Sequence Number | 018698 |
| GCN Sequence Number Description | loratadine TABLET 10 MG ORAL |
| HIC3 | Z2Q |
| HIC3 Description | ANTIHISTAMINES - 2ND GENERATION |
| GCN | 60563 |
| HICL Sequence Number | 007605 |
| HICL Sequence Number Description | LORATADINE |
| Brand/Generic | Generic |
| Proprietary Name | up and up 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 | Target Corporation |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 11673-0612-82 (11673061282)
| NDC Package Code | 11673-612-82 |
|---|---|
| Billing NDC | 11673061282 |
| Package | 1 BOTTLE in 1 CARTON (11673-612-82) / 200 TABLET in 1 BOTTLE |
| Marketing Start Date | 2012-04-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL c4ef0110-89c3-4ded-9a9a-75c0f794f869 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
Other information
Principal Display Panel
CE PACK
Compare to active ingredient in Claritin®
non-drowsy*
allergy relief
loratadine tablets, 10 mg
antihistamine
30 days of relief
original prescription strength
indoor and outdoor allergies
24 hour relief of:
sneezing
runny nose
itchy, watery eyes
itchy throat or nose
24 HOUR
ACTUAL SIZE
30 TABLETS
30 TABLETS
*When taken as directed. See drug facts panel.
INGREDIENTS AND APPEARANCE
| UP AND UP ALLERGY RELIEF
loratadine tablet |
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| Labeler - Target Corporation (006961700) |