MAX TUSSIN MUCUS AND CHEST CONGESTION SUGAR FREE- guaifenesin liquid 
Akron Pharma Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients (in each 10 mL)

Guaifenesin 200 mg

Purposes

Expectorant

Uses

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

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

Other information

Inactive ingredients

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

Questions or comments?

toll-free 1-877-225-6999

Manufactured for:

Akron Pharma, Inc.

Fairfield, NJ 07004

www.akronpharma.com

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MAX TUSSIN MUCUS AND CHEST CONGESTION SUGAR FREE 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0024
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71399-0024-41 in 1 PACKAGE05/15/2023
1118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:71399-0024-81 in 1 PACKAGE05/15/2023
2236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:71399-0024-6473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34105/15/2023
Labeler - Akron Pharma Inc. (067878881)

Revised: 5/2023
Document Id: 73570cd5-b309-447d-ac71-b3f9d417b918
Set id: 3b023b91-e703-4599-9864-96d8c328b45c
Version: 1
Effective Time: 20230515
 
Akron Pharma Inc.