SEVERE CONGESTION AND COUGH MAX- dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid 
AptaPharma Inc.

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Maximum strength Max Severe Congestion & Cough

Drug Facts


Active ingredients
(in each 20 mL)
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Phenylephrine HCl 10 mg

Purpose

Dextromethorphan HBr    Cough suppressant
Guaifenesin                     Expectorant
Phenylephrine                 Nasal Decongestant

Uses
● 
helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
● temporarily relieves these symptoms occurring with a cold:
      ● cough due to minor throat and bronchial irritation
      ● nasal congestion

Warnings

         • Do not use ● if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for
            depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI
            drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking
            this product.
For children under 12 years of age

Ask a doctor before use if you have ● heart disease ● thyroid disease ● high blood pressure ● diabetes
● trouble urinating due to an enlarged prostate gland ● cough that lasts or is chronic such as occurs with smoking,
asthma, chronic bronchitis or emphysema ● cough that occurs with too much phlegm (mucus)

When using this product do not use more than directed

Stop use and ask a doctor if
●nervousness, dizziness or sleeplessness occur ● symptoms do not get better within 7 days or are accompanied by a
fever ● cough comes back, or occurs with 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.

Directions
• take only as recommended
• use dosage cup
• mL =milliliter
• do not take more than 6 doses in any 24-hour period

Age                                         Dose
 Adults & children 12 years and older 20 mL every 4 hours
 Children under 12 years of age Do not use

Other information
each 20 mL contains: sodium 10 mg
dosage cup provided
store between 15-30°C (59-86°F)
do not refrigerate

Inactive ingredients
Anhydrous citric acid, edetate disodium, FD&C Blue # 1, FD&C Red # 40, flavors, glycerin, propylene glycol, propyl
gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Questions? Call weekdays from 9:30AM to 4:30 PM EST 1-877-798-5944

Maximum Strength Max Severe Congestion & Cough

AP SAFE®                   NDC 76281-517-25

Compare to Mucinex® FAST-MAX™ Severe Congestion
& Cough Active ingredients*

Maximum Strength
Max Severe Congestion & Cough

Dextromethorphan HBr/
Cough Suppressant
Guaifenesin /Expectorant
Phenylephrine HCI / Nasal Decongestant

Congestion& Cough

Relief of:
• Cough
• Thins & Loosens Mucus
• Nasal & Chest Congestion

Adults- For Ages 12 and over

6 FL OZ ( 177 mL)

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

Manufactured by:
AptaPharma Inc.,
1533 Union Ave.
Pennsauken, NJ 08110

This product is not manufactured or distributed by Reckitt Benckiser Inc., distributor of Mucinex® FAST-MAX™ Severe
Congestion & Cough.

517 6 Oz

res

SEVERE CONGESTION AND COUGH MAX 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76281-517
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE10 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76281-517-25177 mL in 1 BOTTLE; Type 0: Not a Combination Product01/30/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01201/30/2024
Labeler - AptaPharma Inc. (790523323)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(76281-517)

Revised: 1/2024
Document Id: 1758bfe6-e9c6-445d-9a3c-55c24ba5bde1
Set id: 17a07d2d-f2da-4e51-9a77-6f0c174987bb
Version: 1
Effective Time: 20240131
 
AptaPharma Inc.