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Medi-First Cold Relief (Unifirst First Aid Corporation)

Available Formats

Dosage Form Package Information Links
TABLET, FILM COATED 50 PACKET in 1 BOX, UNIT-DOSE (47682-139-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-139-99) Label Information
TABLET, FILM COATED 125 PACKET in 1 BOX, UNIT-DOSE (47682-139-48) > 2 TABLET, FILM COATED in 1 PACKET (47682-139-99) Label Information
TABLET, FILM COATED 250 PACKET in 1 BOX, UNIT-DOSE (47682-139-13) > 2 TABLET, FILM COATED in 1 PACKET (47682-139-99) Label Information

Complete Medi-First Cold Relief Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredients (in each tablet)

    Acetaminophen 325 mg

    Dextromethorphan Hydrobromide 15mg

    Guaifenesin 200mg

    Phenylephrine Hydrochloride 5mg


  • Purposes

    Pain reliever/ fever reducer

    Cough suppressant

    Expectorant

    Nasal decongestant


  • Uses

    Temporarily relieves these cold symptoms

    • cough
    • sore throat
    • minor aches and pains
    • headache
    • nasal congestion
    • helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

    Temporarily reduces fever.


  • Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 4,000 mg of acetaminophen in 24 hours
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Allergy alert:

    Acetaminophen may cause severe skin reactions. Symptoms may include:

    â–  skin reddening

    â–  blisters

    â–  rash

    If a skin reaction occurs, stop use and seek medical help right away.

    Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

    Do not use
    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if you have ever had an allergic reaction to this product or any of its ingredients
    • 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
    • liver disease
    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • trouble urinating due to an enlarged prostate gland
    • cough that occurs with too much phlegm (mucus)
    • persistent or chronic cough that lasts as occurs with smoking, asthma, chronic bronchitis or emphysema

    Ask a doctor or pharmacist before use if you are
    • taking the blood thinning drug warfarin

    When using this product
    • do not use more than directed

    Stop use and ask a doctor if
    • new symptoms occur
    • redness or swelling is present
    • pain or nasal congestion gets worse or lasts for more than 7 days
    • fever gets worse or lasts for more than 3 days
    • you get nervous, dizzy or sleepless
    • cough comes back or occurs with rash or headache that lasts.

    These could be signs of a serious condition.

    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. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.


  • Directions

    Adults and children: (12 years and older)

    Take 2 tablets with water every 6- 8 hours as needed. Do not take more than 8 tablets in 24 hours.

    Children under 12 years:

    Do not give to children under 12 years of age.


  • Other information

    • store at room temperature 59°-86°F (15°-30°C)
    • avoid excessive heat and humidity
    • tamper evident sealed packets
    • do not use any opened or torn packets

  • Inactive ingredients

    maltodextrin, microcrystalline cellulose, povidone, silicon dioxide*, sodium starch glycolate, starch, stearic acid

    *May contain


  • Questions or comments?

    1-800-634-7680


  • Medique Decorel Forte Plus Label

    Medique®

    Decorel Forte Plus

    Severe Cold & Cough Relief

    Aches, Fever Reducer Acetaminophen 325mg

    Coughs Dextromethorphan HBr 15mg

    Chest Congestion Guaifenesin 200mg

    Nasal Congestion Phenylephrine HCl 5mg

    Pull to Open

    100 Tablets

    (50 x 2)

    Tamper Evident Unit Dose Packets

    Medique Decorel Forte Plus Label


  • Medi-First Cold Relief Label

    Medi-First®

    Cold Relief Multi-Symptom

    100 Tablets

    (50 x 2)

    Aches, Fever Acetaminophen 325mg

    Cough Dextromethorphan HBr 15mg

    Chest Congestion Guaifenesin 200mg

    Nasal Congestion Phenylephrine HCl 5mg

    Pull to Open

    Multy-Symptom Relief

    Pain Reliever/Fever Reducer Cough Suppressant

    Tamper Evident Unit Dose Packets

    Medi-First Cold Relief Label


  • Medi-First Plus Cold Relief Label

    100 Tablets

    (50 x 2's)

    Medi-First® Plus

    Cold Relief

    Acetaminophen 325mg

    Dextromethorphan HBr 15mg, Guaifenesin, Phenylephrine HCl 5mg

    Pull to Open

    Multi-Symptom

    Tamper Evident Unit Dose Packets

    Medi-Forst Plus Cold relieflabel


  • INGREDIENTS AND APPEARANCE
    MEDIQUE DECOREL FORTE PLUS 
    acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-138
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (ROUND) Size 12mm
    Flavor Imprint Code FR;12
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-138-33 50 in 1 BOX 12/30/2008
    1 NDC:47682-138-99 2 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-138-13 250 in 1 BOX 12/30/2008
    2 NDC:47682-138-99 2 in 1 PACKET; Type 0: Not a Combination Product
    3 NDC:47682-138-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 12/30/2008
    MEDI-FIRST COLD RELIEF 
    acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-139
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (ROUND) Size 12mm
    Flavor Imprint Code FR;12
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-139-33 50 in 1 BOX 12/30/2008
    1 NDC:47682-139-99 2 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-139-48 125 in 1 BOX 12/30/2008
    2 NDC:47682-139-99 2 in 1 PACKET; Type 0: Not a Combination Product
    3 NDC:47682-139-13 250 in 1 BOX 12/30/2008
    3 NDC:47682-139-99 2 in 1 PACKET; Type 0: Not a Combination Product
    4 NDC:47682-139-99 2 in 1 PACKET; Type 0: Not a Combination Product 12/30/2008
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 12/30/2008
    MEDI-FIRST PLUS COLD RELIEF 
    acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-159
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color white (white) Score no score
    Shape ROUND (ROUND) Size 12mm
    Flavor Imprint Code FR;12
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-159-33 50 in 1 BOX 12/30/2008
    1 2 in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:47682-159-48 125 in 1 BOX 12/30/2008
    2 2 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 12/30/2008
    Labeler - Unifirst First Aid Corporation (832947092)
    Establishment
    Name Address ID/FEI Business Operations
    Prestige Packaging 170837962 relabel(47682-138, 47682-139, 47682-159) , repack(47682-138, 47682-139, 47682-159)