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Rescon GG (Capellon Pharmaceuticals, LLC)

Available Formats

Dosage Form Package Information Links
LIQUID 25 mL in 1 BOTTLE (64543-044-01) Label Information
LIQUID 118 mL in 1 BOTTLE (64543-044-04) Label Information
LIQUID 473 mL in 1 BOTTLE (64543-044-16) Label Information

Complete Rescon GG Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredients (in each 5 mL teaspoonful)

    Guaifenesin, USP 100 mg

    Phenylephrine HCl 5 mg


  • Purpose

    Guaifenesin Expectorant

    Phenylephrine HCl Nasal decongestant


  • 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 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 two 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 drug.


  • Ask a doctor before use if you have

    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • 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 excessive phlegm (mucus)

  • When using this product

    do not exceed the recommended dosage


  • Stop use and ask a doctor if

    • nervousness, dizziness, or sleeplessness occur.
    • cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache. These could be signs of a serious condition.

  • If pregnant or breast-feeding,

    ask a health professional before use.


  • Keep out of the reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.


  • Directions

    Age Dose
    Adults and children over 12 years of age 2 teaspoonsful (10 mL) every 4 hours
    Children 6 to under 12 years of age 1 teaspoonsful (5 mL) every 4 hours
    Children 2 to under 6 years of age 1/2 teaspoonsful (2.5 mL) every 4 hours
    Children under 2 years of age Ask your doctor

    Do not exceed 6 doses in a 24-hour period


  • Other information

    • store at 20°- 25°C (68°- 77°F)
    • tamper evident: do not use if foil seal under the cap is broken or missing.
    • contains less than 1 mg sodium in each 5 mL teaspoonful

  • Inactive Ingredients

    artificial flavors, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sorbitol, and sugar.


  • Questions or Comments

    Serious side effects may be reported to this number, call (817) 595-5820 (8 am to 5 pm CST).


  • Package Label

    Figure 1: 16 oz. bottle label

    figure-01

  • INGREDIENTS AND APPEARANCE
    RESCON GG  
    guaifenesin and phenylephrine hydrochloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:64543-044
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg  in 5 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SORBITOL (UNII: 506T60A25R)  
    SUCROSE (UNII: C151H8M554)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor CHERRY (WILD) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64543-044-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1999
    2 NDC:64543-044-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1999
    3 NDC:64543-044-01 25 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/1999
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 01/01/1999
    Labeler - Capellon Pharmaceuticals, LLC (124568093)