NDC 46122-650 Nasal Decongestant
Phenylephrine Hcl Tablet, Film Coated Oral
Product Information
What is NDC 46122-650?
The NDC code 46122-650 is assigned by the FDA to the product Nasal Decongestant which is a human over the counter drug product labeled by Amerisource Bergen. The generic name of Nasal Decongestant is phenylephrine hcl. The product's dosage form is tablet, film coated and is administered via oral form. The product is distributed in a single package with assigned NDC code 46122-650-68 2 blister pack in 1 carton / 18 tablet, film coated in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.
What are the uses for Nasal Decongestant?
This medication is used for temporary relief of congestion in the nose caused by various conditions including the common cold, sinusitis, hay fever, and allergies. It works by narrowing the blood vessels in the nose area, reducing swelling and congestion.
Product Characteristics
Color(s) | RED (C48326) |
Shape | ROUND (C48348) |
Size(s) | 7 MM |
Imprint(s) | 44;453 |
Score | 1 |
Product Packages
NDC Code 46122-650-68
Package Description: 2 BLISTER PACK in 1 CARTON / 18 TABLET, FILM COATED in 1 BLISTER PACK
Price per Unit: $0.05022 per EA
Product Details
What are Nasal Decongestant Active Ingredients?
- PHENYLEPHRINE HYDROCHLORIDE 10 mg/1 - An alpha-1 adrenergic agonist used as a mydriatic, nasal decongestant, and cardiotonic agent.
Nasal Decongestant Active Ingredients UNII Codes
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
NDC to RxNorm Crosswalk
- RxCUI: 1049182 - phenylephrine HCl 10 MG Oral Tablet
- RxCUI: 1049182 - phenylephrine hydrochloride 10 MG Oral Tablet
Nasal Decongestant Inactive Ingredients UNII Codes
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
Pharmacologic Class(es)
* Please review the disclaimer below.
Nasal Decongestant Product Label
FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Label Table of Contents
- ACTIVE INGREDIENT (IN EACH TABLET)
- PURPOSE
- USES
- DO NOT USE
- ASK A DOCTOR BEFORE USE IF YOU HAVE
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR IF
- IF PREGNANT OR BREAST-FEEDING,
- KEEP OUT OF REACH OF CHILDREN.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS?
- PRINCIPAL DISPLAY PANEL
Active Ingredient (In Each Tablet)
Phenylephrine HCl 10 mg
Purpose
Nasal decongestant
Uses
- temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
- temporarily relieves sinus congestion and pressure
Do Not Use
if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask A Doctor Before Use If You Have
- heart disease
- diabetes
- thyroid disease
- high blood pressure
- difficulty in urination due to enlargement of the prostate gland
When Using This Product
do not exceed recommended dosage.
Stop Use And Ask A Doctor If
- nervousness, dizziness, or sleeplessness occur
- symptoms do not improve within 7 days or occur with fever
If Pregnant Or Breast-Feeding,
ask a health professional before use.
Keep Out Of Reach Of Children.
In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
- adults and children 12 years and over: take 1 tablet every 4 hours. Do not take more than 6 tablets in 24 hours.
- children under 12 years: ask a doctor
Other Information
- TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
- store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
- see end flap for expiration date and lot number
Inactive Ingredients
croscarmellose sodium, dextrose monohydrate, dibasic calcium phosphate dihydrate, FD&C red #40, lecithin, magnesium stearate, maltodextrin, microcrystalline cellulose, silicon dioxide, sodium carboxymethylcellulose, sodium citrate dihydrate, titanium dioxide
Questions Or Comments?
1-800-426-9391
Principal Display Panel
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PHARMACY®
Compare to Sudafed PE® Congestion active ingredient*
NDC 46122-650-68
MAXIMUM STRENGTH
Nasal Decongestant PE
Phenylephrine HCl 10 mg Nasal Decongestant
Non-drowsy
Relief of:
- Sinus Pressure
- Sinus & Nasal Congestion
36 Tablets
Actual Size
TAMPER EVIDENT: DO NOT USE IS PACKAGE IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
*This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Sudafed PE® Congestion.
50844 ORG011845307
Distributed by
AmerisourceBergen
1300 Morris Drive
Chesterbrook, PA 19087
Questions or Concerns?
www.mygnp.cpm
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