Active ingredients (in each 10 mL)

Guaifenesin 200 mg

Purposes

Expectorant

Uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings

Ask a doctor before use if you have

cough that occurs with too much phlegm (mucus)
cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

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 take more than 6 doses in any 24-hour period
measure only with dosing cup provided
mL= milliliter
this adult product is not intended for use in children under 12 years of age


age	dose
adults and children 12 years and over	10 - 20 mL every 4 hours
children under 12 years	do not use

Other information

Phenylketonurics: contains Phenylalanine 30 mg per 10 mL
store at 20-25ºC(68-77ºF). Do not refrigerate

Inactive ingredients

anhydrous citric acid, flavor cherry, glycerin, menthol, purified water, saccharin sodium, sodium benzoate, sorbitol solution, sucralose, sucrose.

Questions or comments?

toll-free 1-877-225-6999

Manufactured for:

Akron Pharma, Inc.

Fairfield, NJ 07004

www.akronpharma.com

8Oz

MAX TUSSIN MUCUS AND CHEST CONGESTION
guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71399-0054
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg in 10 mL

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71399-0054-8	1 in 1 PACKAGE	11/03/2023
1		236 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	11/03/2023

Labeler - Akron Pharma Inc. (067878881)

Registrant - HI-TECH PHARMACEUTICALS PRIVATE LIMITED (862584260)

Name	Address	ID/FEI	Business Operations
Establishment
HI-TECH PHARMACEUTICALS PRIVATE LIMITED		862584260	manufacture(71399-0054)

MAX TUSSIN MUCUS & Chest CongestionExpectorant Drug Facts