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NDC 00113-0325-66 Good Sense Mucus ER 1200 mg/1 Details

Good Sense Mucus ER 1200 mg/1

Good Sense Mucus ER is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by L. Perrigo Company. The primary component is GUAIFENESIN.

MedlinePlus Drug Summary

Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.

Related Packages: 00113-0325-66
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Guaifenesin

Product Information

NDC	00113-0325
Product ID	0113-0325_21d817c7-887b-4e6d-a22b-0a9dc15bc822
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Good Sense Mucus ER
Proprietary Name Suffix	n/a
Non-Proprietary Name	Guaifenesin
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	1200
Active Ingredient Units	mg/1
Substance Name	GUAIFENESIN
Labeler Name	L. Perrigo Company
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA091009
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00113-0325-66 (00113032566)

Pricing Information	N/A
NDC Package Code	0113-0325-66
Billing NDC	00113032566
Package	1 BOTTLE in 1 CARTON (0113-0325-66) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
Marketing Start Date	2017-09-19
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 8dcd36a1-4d3b-4435-9b6b-a2428b5c6744 Details

Active ingredient (in each extended-release tablet)

Guaifenesin 1200 mg

Purpose

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Warnings

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).

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: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.
•: children under 12 years of age: do not use

Other information

•: store between 20°-25°C (68°-77°F)
•: do not use if printed foil under cap is broken or missing

Inactive ingredients

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?

1-800-719-9260

Package/Label Principal Display Panel

12 Hour

Maximum Strength

Mucus - ER

Guaifenesin Extended-Release Tablets, 1200 mg

Expectorant

Relieves Chest Congestion

Thins and Loosens Mucus

Compare to active ingredient of Maximum Strength Mucinex®

100% SATISFACTION GUARANTEED

14 Extended-Release Tablets

INGREDIENTS AND APPEARANCE

GOOD SENSE MUCUS ER

guaifenesin tablet, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0113-0325
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	1200 mg

Ingredient Name	Strength
Inactive Ingredients
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
COPOVIDONE K25-31 (UNII: D9C330MD8B)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	BLUE (Light Blue)	Score	no score
Shape	OVAL (Biconvex)	Size	22mm
Flavor		Imprint Code	Watson;1200
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0113-0325-66	1 in 1 CARTON	09/19/2017
1		14 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA091009	09/19/2017

Labeler - L. Perrigo Company (006013346)

Revised: 12/2019

Document Id: 21d817c7-887b-4e6d-a22b-0a9dc15bc822

Set id: 8dcd36a1-4d3b-4435-9b6b-a2428b5c6744

Version: 2

Effective Time: 20191206