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Nasal Decongestant by H E B

Medically reviewed on February 6, 2018

Dosage form: tablet, film coated
Ingredients: PSEUDOEPHEDRINE HYDROCHLORIDE 30mg
Labeler: H E B
NDC Code: 37808-112

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.

HEB 44-112

Active ingredient (in each tablet)

Pseudoephedrine HCl 30 mg

Purpose

Nasal decongestant

Uses
  • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • temporarily relieves sinus congestion and pressure

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.

Ask a doctor before use if you have
  • diabetes
  • heart disease
  • high blood pressure
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland

When using this product

do not exceed recommended dose. 

Stop use and ask a doctor if
  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not improve within 7 days or occur with fever

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
adults and children 12 years and older take 2 tablets every 4 to 6 hours; do not take more than 8 tablets in 24 hours
children ages 6 to 12 yearstake 1 tablet every 4 to 6 hours; do not take more than 4 tablets in 24 hours
children under 6 yearsdo not use this product in children under 6 years of age

Other information
  • store at 25ºC (77ºF); excursions permitted between15º-30ºC (59º-86ºF)
  • see end flap for expiration date and lot number

Inactive ingredients

croscarmellose sodium, dicalcium phosphate, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, silica gel, titanium dioxide, triacetin

Questions or comments?

1-800-426-9391

Principal display panel

Compare to Sudafed® Congestion active ingredient*

NDC 37808-112-22

H • E • B ®

Maximum Strength
NASAL DECONGESTANT

Pseudoephedrine HCl 30 mg /
Nasal Decongestant

Sinus Pressure & Congestion

Non-Drowsy 

Relief of:
• Nasal & Sinus Congestion
• Sinus Pressure

actual size

48 TABLETS, 30 mg EACH

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

*This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Sudafed® Congestion.
50844     ORG071211222    

DOES NOT CONTAIN GLUTEN

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.

MADE WITH PRIDE AND CARE FOR H-E-B®, SAN ANTONIO, TX 78204

HEB 44-112

NASAL DECONGESTANT 
pseudoephedrine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-112
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS 
CELLULOSE, MICROCRYSTALLINE 
CROSCARMELLOSE SODIUM 
MAGNESIUM STEARATE 
SILICON DIOXIDE 
POLYDEXTROSE 
HYPROMELLOSE, UNSPECIFIED 
FD&C RED NO. 40 
TRIACETIN 
FD&C YELLOW NO. 6 
TITANIUM DIOXIDE 
POLYETHYLENE GLYCOL, UNSPECIFIED 
Product Characteristics
ColorREDScoreno score
ShapeROUNDSize7mm
FlavorImprint Code44;112
Contains    
Packaging
#Item CodePackage Description
1NDC:37808-112-222 BLISTER PACK in 1 CARTON
124 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34108/25/1981
Labeler - H E B (007924756)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(37808-112)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(37808-112)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(37808-112)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(37808-112)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(37808-112)

 
H E B

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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