NDC | 30142-144-68, 30142-144-89 |
Set ID | 23076826-beba-4f56-b298-6efa07adef98 |
Category | HUMAN OTC DRUG LABEL |
Packager | Kroger Company |
Generic Name | |
Product Class | alpha-Adrenergic Agonist |
Product Number | |
Application Number | ANDA091071 |
- Active ingredients (in each extended-release tablet)
- Purpose
-
Uses
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- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
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- temporarily relieves nasal congestion due to:
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- common cold
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- hay fever
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- upper respiratory allergies
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- temporarily restores freer breathing through the nose
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- promotes nasal and/or sinus drainage
- •
- temporarily relieves sinus congestion and pressure
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Warnings
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
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- heart disease
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- high blood pressure
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- thyroid disease
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- diabetes
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- trouble urinating due to an enlarged prostate gland
- •
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- •
- cough accompanied by too much phlegm (mucus)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
COMPARE TO the active ingredients of MUCINEX® D See back panel
OUR PHARMACIST RECOMMENDED
Mucus-D
Guaifenesin 600 mg / Pseudoephedrine Hydrochloride 60 mg Extended-Release Tablets
EXPECTORANT/NASAL DECONGESTANT
Clears Nasal/Sinus Congestion
Thins & Loosens Mucus
actual size
12 HOUR
18 EXTENDED-RELEASE TABLETS
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INGREDIENTS AND APPEARANCE
MUCUS D
guaifenesin, pseudoephedrine hydrochloride tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-144 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) COPOVIDONE K25-31 (UNII: D9C330MD8B) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color ORANGE (peach) Score no score Shape OVAL (biconvex) Size 18mm Flavor Imprint Code 600;Watson Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-144-68 2 in 1 CARTON 04/20/2017 1 18 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:30142-144-89 1 in 1 CARTON 04/20/2017 2 18 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA091071 04/20/2017 Labeler - Kroger Company (006999528)