Label: GUAIFENESIN AND PSEUDOEPHEDRINE HCL tablet, extended release
- NDC Code(s): 0363-0134-78
- Packager: WALGREEN CO.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 20, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purposes
-
Uses
- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
- temporarily relieves nasal congestion due to:
- common cold
- hay fever
- upper respiratory allergies
- temporarily restores freer breathing through the nose
- promotes nasal and/or sinus drainage
- temporarily relieves sinus congestion and pressure
-
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
- 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?
-
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1200 mg/120 mg (24 Tablet Carton Label)
walgreens
Compare to the active
ingredients in Mucinex®D††
NDC 0363-0134-78
MAXIMUM STRENGTH
Mucus Relief D
GUAIFENESIN USP 1200 mg / EXPECTORANT
PSEUDOEPHEDRINE HCl USP 120 mg / NASAL DECONGESTANT
EXTENDED-RELEASE TABLETS
Maximum Strength 12 Hour
• Clears nasal/sinus congestion
• Thins & loosens mucus
24
EXTENDED-
RELEASE
TABLETS ACTUAL SIZE
-
INGREDIENTS AND APPEARANCE
GUAIFENESIN AND PSEUDOEPHEDRINE HCL
guaifenesin and pseudoephedrine hcl tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0134 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK) MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y) POVIDONE K25 (UNII: K0KQV10C35) POVIDONE K90 (UNII: RDH86HJV5Z) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color WHITE (white to off-white) Score no score Shape CAPSULE (modified, biconvex) Size 22mm Flavor Imprint Code 65;X Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0134-78 2 in 1 CARTON 08/05/2020 1 12 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 ANDA213203 08/05/2020 Labeler - WALGREEN CO. (008965063) Registrant - Aurohealth LLC (078728447) Establishment Name Address ID/FEI Business Operations APL HEALTHCARE LIMITED 650918514 ANALYSIS(0363-0134) , MANUFACTURE(0363-0134)