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NDC 69842-0017-24 Allergy Relief 12 mg/1 Details
Allergy Relief 12 mg/1
Allergy Relief is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is CHLORPHENIRAMINE MALEATE.
MedlinePlus Drug Summary
Chlorpheniramine relieves red, itchy, watery eyes; sneezing; itchy nose or throat; and runny nose caused by allergies, hay fever, and the common cold. Chlorpheniramine helps control the symptoms of cold or allergies but will not treat the cause of the symptoms or speed recovery. Chlorpheniramine 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.
Related Packages: 69842-0017-24Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Chlorpheniramine
Product Information
| NDC | 69842-0017 |
|---|---|
| Product ID | 69842-017_e6e972a9-298c-488a-b9fc-2bcce75c289b |
| 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 | Chlorpheniramine Maleate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 12 |
| Active Ingredient Units | mg/1 |
| Substance Name | CHLORPHENIRAMINE MALEATE |
| Labeler Name | CVS Pharmacy |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040829 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 69842-0017-24 (69842001724)
| NDC Package Code | 69842-017-24 |
|---|---|
| Billing NDC | 69842001724 |
| Package | 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 CARTON (69842-017-24) |
| Marketing Start Date | 2011-01-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 626aa162-f5e3-45c0-b5ac-d70bff255aed Details
USES
WARNINGS
Ask a doctor before use if you have
a breathing problem such as emphysema or chronic bronchitis
glaucoma
trouble urinating due to an enlarged prostate gland
Ask a doctor or pharmacist before use if you are
taking sedatives or tranquilizers
When using this product
excitability may occur, especially in children
drowsiness may occur
avoid alcoholic beverages
alchohol, sedatives and tranquilizers may increase drowsiness
use caution when driving a motor vehicle or operating machinery
Call your doctor for medical advice about side effects.
You may report side effects to FDA at 1-800-FDA-1088
If pregnant or breast-feeding, ask a health professional before use
KEEP OUT OF REACH OF CHILDREN
DIRECTIONS
OTHER INFORMATION
INACTIVE INGREDIENTS
calcium sulfate, carnauba wax, colloidal silicon dioxide, confectioner’s sugar, D&C yellow No. 10 aluminum lake, FD&C blue No. 2/indigo carmine aluminum lake, FD&C yellow No. 6, gelatin, hydroxypropyl methylcellulose, lactose monohydrate, magnesium stearate, methacrylic acid copolymer, methyl parahydroxybenzoate, microcrystalline cellulose, pharmaceutical ink, polysorbate 80, povidone, propyl parahydroxybenzoate, propylene glycol, sodium benzoate, sodium lauryl sulphate, sucrose, talc, titanium dioxide, triethyl citrate
PURPOSE
Principal Display Panel
INGREDIENTS AND APPEARANCE
| ALLERGY RELIEF
chlorpheniramine maleate tablet, film coated, extended release |
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| Labeler - CVS Pharmacy (062312574) |