- 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 or comments?
-
Principal Display Panel
Compare to Maximum Strength Mucinex® active ingredient††
12 HOUR
Mucus Relief ER
GUAIFENESIN EXTENDED-RELEASE
TABLETS, 1200 mg / EXPECTORANT
MAXIMUM STRENGTH
12 HOUR
- Relieves Chest Congestion
- Thins & Loosens Mucus
EXTENDED-RELEASE TABLETS
††This product is not manufactured or distributed by Reckitt Benckiser LLC, distributor of Maximum Strength 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: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Package Label
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF EXTENDED RELEASE MAXIMUM STRENGTH
guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0832 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 22mm Flavor Imprint Code AN037 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0832-14 14 in 1 CARTON 08/31/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-0832-28 28 in 1 CARTON 08/31/2018 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 08/31/2018 Labeler - Walgreens (008965063)