- 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 accopanied by too much phlegm (mucus)
- Directions
- Other information
- Inactive ingredients
- Questions?
-
Principal Display Panel
Compare to active ingredient in Maximum Strength Mucinex®*
maximum strength
mucus relief
guaifenesin 1200 mg
expectorant
relieves Chest Congestion
thin & Loosens Mucus
EXTENDED-RELEASE TABLETS
*This product is not manufactured or distributed by Reckitt Benckiser LLC, distributor of Maximum Strength Mucinex®.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
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:11673-732 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 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 6mm Flavor Imprint Code AN037 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-732-14 14 in 1 CARTON 07/11/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11673-732-28 28 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)