- Active ingredient (in each extended-release tablet)
- Purpose
- Uses
-
Warnings
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)
-
Directions
- 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: take 1 or 2 tablets every 12 hours. Do not exceed 4 tablets in 24 hours
- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Question?
-
Principal Display Panel
Compare to active ingredient in Mucinex®*
Mucus Relief
Guaifenesin 600 mg
Expectorant
relieves chest congestion
thin and loosens mucus
EXTENDED-RELEASE TABLETS
*This product is not manufactured or distributed by Reckitt Benckiser LLC, distributor of Mucinex®.
TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN, OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by Target Corporation
Minneapolis, MN 55403
TM & ©2018 Target Brands, Inc.
- Package Label
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF EXTENDED-RELEASE
guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-731 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) CARBOMER 934 (UNII: Z135WT9208) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color BLUE Score no score Shape OVAL Size 16mm Flavor Imprint Code AN036 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-731-40 40 in 1 CARTON 07/11/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11673-731-20 20 in 1 CARTON 07/11/2018 2 1 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 ANDA207342 07/11/2018 Labeler - TARGET Corporation (006961700)