OTC Target Corporation Up and Up mucus relief
Up and Up mucus relief by Target Corporation
Medically reviewed on Jul 13, 2018
Dosage form: tablet, extended release
Ingredients: GUAIFENESIN 1200mg Labeler: Target Corporation NDC Code: 11673-325
Target Corporation Mucus Relief Drug Facts
Active ingredient (in each extended-release tablet)
Guaifenesin 1200 mg
helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
Do not use
for children under 12 years of age
Ask a doctor before use if you have
persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
cough accompanied by too much phlegm (mucus)
Stop use and ask a doctor if
cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache.
These could be signs of a serious illness.
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).
do not crush, chew, or break tablet
take with a full glass of water
this product can be administered without regard for the timing of meals
adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.
children under 12 years of age: do not use
store between 20
°-25 °C (68 °-77 °F) •
do not use if printed foil under cap is broken or missing
colloidal silicon dioxide, copovidone, FD&C blue #1 aluminum lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, sodium starch glycolate Type A, stearic acid
Questions or comments?
Package/Label Principal Display Panel
Compare to active ingredient in Maximum Strength Mucinex®
guaifenesin extended-release tablets, 1200 mg
relieves chest congestion
thins land loosens mucus
28 EXTENDED-RELEASE TABLETS
UP AND UP MUCUS RELIEF
guaifenesin tablet, extended release
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-325
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 1200 mg
Ingredient Name Strength
FD&C BLUE NO. 1
Color BLUE (Light Blue) Score no score
Shape OVAL (Biconvex) Size 22mm
Flavor Imprint Code Watson;1200
# Item Code Package Description
1 NDC:11673-325-66 1 BOTTLE in 1 CARTON
1 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
2 NDC:11673-325-30 1 BOTTLE in 1 CARTON
2 28 TABLET, EXTENDED RELEASE in 1 BOTTLE
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091009 07/11/2016
Labeler - Target Corporation
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