MAX COLD, FLU, AND SORE THROAT- acetaminophen,dextromethorphan hydrobromide, guaifenesin , phenylephrine hcl liquid 
H E B

----------

Drug Facts Active ingredients

Active ingredients (in each 20 mL)

Acetaminophen 650 mg
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Phenylephrine HCL 10 mg

Purpose

Pain reliever/Fever reducer
Cough suppressant
Expectorant
Nasal Decongestant

Keep out of reach of children.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right awaay.

Uses

temporarily relieves these common cold and flu symptoms:


Warnings

Liver warning This product contains
acetaminophen. Severe liver damage
may occur if you take: ■ more than
4,000 mg of acetaminophen in 24 hours
■ with other drugs containing
acetaminophen
■ 3 or more alcoholic drinks daily while
using this product

Allery Alert: Acetaminophen may cause
severe skin reaction. Symptoms may include:
■ skin reddening - blisters ■ rash
If a skin reaction occurs, stop use and
seek medical help right away.           

Sore throat warning If sore throat
is severe, persists for more than 2
days, is accompanied or followed
by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

Do not use

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast feeding

ask a health professional before use.

Overdose warning

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact the Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Age                                                                                  Dose

Adults and children 12 years and older                                20 mL every 4 hours

Children under 12 years of age                                           Do not use


Other information

Inactive ingredients

 Anhydrous citric acid, edetate disodium, FD and C Blue #1, FD and 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™ 

Cold, Flu & Sore Throat active ingredients*

                                    NDC 37808-316-25

H E B®

Maximum Strength

MAX COLD, FLU & SORE THROAT

Acetaminophen /
(Pain Reliver/Fever Reducer)
Dextromethorphan HBr /
(Cough Suppressant)
Guaifensin / (Expectorant)
Phenylephrine HCL /
Nasal Decongestant)

Cold, Flu & Throat


Relief of:
• Fever and Body aches
• Controls Cough
• Thins and Loosens Mucus
• Relieves Nasal and Chest Congestion

Adults
For ages 12 and Over

6 FL OZ (117 mL)              LF-002 Rev.2 02

Peel Corner to Read Complete Drug Facts and Information

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING
Failure to follow these warnings could result in consequences

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-002 Rev 02

               1208

Lot:
Exp:


HEB MaxCold pg1

HEB MaxCold pg2

HEB MaxCold pg3

MAX COLD, FLU, AND SORE THROAT 
acetaminophen,dextromethorphan hydrobromide, guaifenesin , phenylephrine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-316
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 20 mL
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:37808-316-25117 mL in 1 BOTTLE; Type 0: Not a Combination Product03/05/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01303/05/2014
Labeler - H E B (007924756)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(37808-316)

Revised: 12/2023
Document Id: 0d19111b-d15e-4e5d-a9e1-5403e7509902
Set id: 9b09b660-0758-48dc-84c9-26cdd2aacc03
Version: 3
Effective Time: 20231229
 
H E B