Label: GOOD SENSE MUCUS ER- guaifenesin tablet, multilayer, extended release
- NDC Code(s): 0113-3650-00, 0113-3650-01, 0113-3650-10, 0113-3650-74
- Packager: L. Perrigo Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated February 21, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each extended-release tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
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- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
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- cough accompanied by too much phlegm (mucus)
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Directions
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- do not crush, chew, or break tablet
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- take with a full glass of water
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- this product can be administered without regard for the timing of meals
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- adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.
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- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
GOODSENSE®
12 Hour
Maximum Strength
Mucus•ER
Guaifenesin Extended-Release Tablets, 1200 mg
Actual Size
Expectorant
• Relieves Chest Congestion
• Thins and Loosens Mucus
• Immediate and Extended Release
Compare to active ingredient of Maximum Strength Mucinex®
BONUS SIZE 7 + 7 Tablets FREE
14 Extended-Release Tablets
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INGREDIENTS AND APPEARANCE
GOOD SENSE MUCUS ER
guaifenesin tablet, multilayer, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-3650 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 CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) (UNII: K6MOM3T5YL) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color WHITE Score no score Shape OVAL Size 22mm Flavor Imprint Code G;1200 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-3650-74 1 in 1 CARTON 03/20/2021 1 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0113-3650-01 2 in 1 CARTON 09/09/2021 2 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0113-3650-00 1 in 1 CARTON 03/31/2022 3 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:0113-3650-10 7 in 1 CARTON 05/05/2022 05/05/2022 4 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 ANDA213420 03/20/2021 Labeler - L. Perrigo Company (006013346)