GUAIFENESIN tablet, extended release

Guaifenesin by

Drug Labeling and Warnings

Guaifenesin by is a Otc medication manufactured, distributed, or labeled by Aurohealth LLC, Aurobindo Pharma Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

(in each extended-release tablet)
 Guaifenesin USP 600 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 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

• store between 20° to 25°C (68° to 77°F)
• Tamper evident: Do not use if carton is open or if seal on blister is broken or missing

Inactive ingredients

colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinised starch (maize)

Questions?

1-855-274-4122 (Monday – Friday 8:30 AM to 5:00 PM EST) You may also report side effects to this phone number.

Distributed by:
Aurohealth LLC.
2572 Brunswick Pike,
Lawrenceville, NJ 08648

Code: AP/DRUGS/04/2016

Made in India

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 600 mg (20 Tablet Label)

AUROHEALTH

NDC: 58602-810-73

Guaifenesin
Extended-Release
Tablets 600 mg

EXPECTORANT 

12 HOUR

• Relieves Chest Congestion
• Thins And Loosens Mucus

20 
Extended-Release
Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 600 mg (20 Tablet Carton Label)

AUROHEALTH

NDC: 58602-810-73

Compare to the active
ingredient in Mucinex®*

Guaifenesin
Extended-release Tablets 600 mg

EXPECTORANT
 
Relieves Chest Congestion
Thins And Loosens Mucus

12 HOUR 

 20 Extended Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 600 mg Blister Carton (20 (1 x 20) Tablets)

AUROHEALTH

NDC: 58602-810-96

Compare to the active
ingredient in Mucinex®*

Guaifenesin
Extended-release Tablets 600 mg

EXPECTORANT
 
Relieves Chest Congestion
Thins And Loosens Mucus

20
Extended-Release
Tablets

12 HOUR 

INGREDIENTS AND APPEARANCE

GUAIFENESIN 
guaifenesin tablet, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58602-810
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)
HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
HYPROMELLOSE 2910 (10000 MPA.S) (UNII: 0HO1H52958)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y)
POVIDONE K90 (UNII: RDH86HJV5Z)
POVIDONE K25 (UNII: K0KQV10C35)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	WHITE (white to off-white)	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code	L;68
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58602-810-73	1 in 1 CARTON	10/21/2019
1		20 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 58602-810-12	1 in 1 CARTON	10/21/2019
2		40 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 58602-810-21	1 in 1 CARTON	10/21/2019
3		100 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 58602-810-96	1 in 1 CARTON	10/21/2019
4		20 in 1 BLISTER PACK; Type 0: Not a Combination Product
5	NDC: 58602-810-97	2 in 1 CARTON	10/21/2019
5		20 in 1 BLISTER PACK; Type 0: Not a Combination Product
6	NDC: 58602-810-98	5 in 1 CARTON	10/21/2019
6		20 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	ANDA210453	10/21/2019

Labeler - Aurohealth LLC (078728447)

Establishment
Name	Address	ID/FEI	Business Operations
Aurobindo Pharma Limited		650918514	ANALYSIS(58602-810) , MANUFACTURE(58602-810)