Available Formats

• Active ingredient (in each 10 mL)

  Guaifenesin, USP 200 mg

  ---

• Purpose

  Expectorant

  ---

• Use

  helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

  ---

• Warnings

  Ask a doctor before use if you have

  • cough that occurs with too much phlegm (mucus)

  • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

  Stop use and ask a doctor if

  cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign 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 (1-800-222-1222).

  ---

• Directions

  • do not take more than 6 doses in any 24-hour period

  • measure only with dosing cup provided

  • keep dosing cup with product

  • mL = milliliter

  • this adult product is not intended for use in children under 12 years of age

  age	dose
  adults and children 12 years and over	10 – 20 mL every 4 hours
  children under 12 years	do not use

  ---

• Other information

  • store at 20-25 °C (68-77 °F). Do not refrigerate.

  ---

• Inactive ingredients

  anhydrous citric acid, caramel, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, maltol, menthol, propylene glycol, purified water, saccharin sodium, sodium benzoate

  ---

• Questions or comments?

  1-800-719-9260

  ---

• Principal Display Panel

  Compare to Robitussin® Mucus + Chest Congestion active ingredient

  ORIGINAL

  Adult Tussin

  Mucus & Chest Congestion

  Guaifenesin (Expectorant)

  Relieves:

  Mucus/Chest Congestion

  For ages 12 & over

  Non-Drowsy

  Gluten Free ● Alcohol Free

  4 Fl oz (118 mL)

  

  ---

• INGREDIENTS AND APPEARANCE

  HEALTH MART ADULT TUSSIN  guaifenesin solution

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62011-0089 Route of Administration ORAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg  in 10 mL

  Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)   CARAMEL (UNII: T9D99G2B1R)   FD&C RED NO. 40 (UNII: WZB9127XOA)   GLYCERIN (UNII: PDC6A3C0OX)   HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)   PROPYLENE GLYCOL (UNII: 6DC9Q167V3)   WATER (UNII: 059QF0KO0R)   SACCHARIN SODIUM (UNII: SB8ZUX40TY)   SODIUM BENZOATE (UNII: OJ245FE5EU)   MALTOL (UNII: 3A9RD92BS4)   MENTHOL (UNII: L7T10EIP3A)

  Product Characteristics Color RED (dark) Score      Shape Size Flavor CHERRY Imprint Code Contains

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62011-0089-1 1 in 1 CARTON 01/11/2012 1 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:62011-0089-2 1 in 1 CARTON 01/04/2013 2 118 mL in 1 BOTTLE; 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 01/11/2012

  Labeler - McKesson (177667227)

  ---