H E B MAX SEVERE CONGESTION AND COUGH MAXIUM STRENGTH- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride  liquid 
H E B

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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 HCL ..........Nasal Decongestant

Uses
• helps loosen phlegm (mucus)
and thin bronchial secretions to
drain bronchial tubes
• temporarily relieves these
symploms 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
oxiclase 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 &               20 ml every 4
children 12               hours
years and
older

Children               Do not use
under 12
years of age

Other information

Inactive ingredients
anhydrous cilric 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 9:30 AM to 4:30 PM EST at

1-877-798-5944

Product Label

Compare to Mucinex® FAST-MAX™

Severe Congestion and Cough active ingredients*

NDC 37808-317-25

H-E-B®

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 & Over

6 FL OZ (177mL)

LF 001 Rev.01

MADE WITH PRIDE AND CARE FOR H-E-B®

SAN ANTONIO, TEXAS, 782044

Peel Corner to Read Complete
Drug Facts and Information →

DO NOT USE IF PRINTED SEAL

UNDER CAP IS TORN OR MISSING

             H-E-B®

100%
GUARANTEE
promise

If you aren't completely pleased
with this product, we'll be happy to
replace it or refund your money.
You have our word on it.


LB·001 Rev.01
            1208
8581-1711

0 41220 38704 5

Lot:
Exp:

*This product is not manufactured or
distributed by Reckill Benckiser Inc..
distributor of Mucinex® FAST-MAXTM
Severe Congeslion &Cough

MADE WITH PRIDE & CARE FOR H·E-B®
SAN ANTONIO. TX 78204

37808-317

res

H E B MAX SEVERE CONGESTION AND COUGH  MAXIUM STRENGTH
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-317
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) PHENYLEPHRINE HYDROCHLORIDE10 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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-317-25177 mL in 1 BOTTLE; Type 0: Not a Combination Product09/14/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01209/14/2012
Labeler - H E B (007924756)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(37808-317)

Revised: 12/2023
Document Id: 9f2c6806-1156-4c91-8581-68b7fcf039ec
Set id: d2b016ee-5329-45bf-9d71-d626204169cf
Version: 4
Effective Time: 20231229
 
H E B