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← See all Nasal Decongestant PE brands

Nasal Decongestant PE by H E B

Dosage form: tablet, film coated
Ingredients: PHENYLEPHRINE HYDROCHLORIDE 10mg
Labeler: H E B
NDC Code: 37808-453

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 44-453

Active ingredient (in each tablet)

Phenylephrine HCl 10 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
  • heart disease
  • diabetes
  • thyroid disease
  • high blood pressure
  • difficulty in urination due to enlargement of the prostate gland 

When using this product do not exceed recommended dose.

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

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 (1-800-222-1222) right away.

Directions
  • adults and children 12 years and over: take 1 tablet every 4 hours. Do not take more than 6 tablets in 24 hours.
  • children under 12 years: ask a doctor

Other information
  • TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN
  • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
  • see end flap for expiration date and lot number 

Inactive ingredients

croscarmellose sodium, dextrose monohydrate, dicalcium phosphate dihydrate, FD&C red #40, lecithin, magnesium stearate, maltodextrin, microcrystalline cellulose, silica gel, sodium carboxymethylcellulose, sodium citrate dihydrate, titanium dioxide

Questions or comments?

1-800-426-9391

Principal Display Panel

Compare to Sudafed PE® Congestion
active ingredient*

NDC 37808-453-23

H • E • B ®

Maximum Strength

NASAL
DECONGESTANT PE
Phenylephrine HCl 10 mg /
Nasal Decongestant

Sinus Decongestant

Non-Drowsy
Relief of:
• Congestion
• Sinus Pressure

actual
size

72 TABLETS

TAMPER EVIDENT: DO NOT USE IF PACKAGE 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 PE® Congestion.

50844     ORG071545323    

DOES NOT CONTAIN GLUTEN

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

100%
GUARANTEE
promise

                 H-E-B®
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.

HEB 44-453

NASAL DECONGESTANT PE 
phenylephrine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-453
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM 
DEXTROSE MONOHYDRATE 
FD&C RED NO. 40 
MAGNESIUM STEARATE 
MALTODEXTRIN 
MICROCRYSTALLINE CELLULOSE 
TITANIUM DIOXIDE 
SILICON DIOXIDE 
CARBOXYMETHYLCELLULOSE SODIUM 
DIBASIC CALCIUM PHOSPHATE DIHYDRATE 
Product Characteristics
ColorREDScoreno score
ShapeROUNDSize7mm
FlavorImprint Code44;453
Contains    
Packaging
#Item CodePackage Description
1NDC:37808-453-233 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 FINALpart34101/14/2005
Labeler - H E B (007924756)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(37808-453)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(37808-453)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867837PACK(37808-453)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.967626305PACK(37808-453)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.868734088PACK(37808-453)

 
H E B

← See all Nasal Decongestant PE brands

Medically reviewed on Feb 1, 2018

Further information

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

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