LORATADINE AND PSEUDOEPHEDRINE SULFATE- loratadine and pseudoephedrine sulfate tablet, film coated, extended release 
HEB

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H-E-B® Allergy Relief-D

Drug Facts

Active ingredients (in each tablet)Purpose
Loratadine, USP 10 mgAntihistamine
Pseudoephedrine sulfate, USP 240 mgNasal decongestant

Uses

Warnings

Do not use

  • if you have ever had an allergic reaction to this product or any of its ingredients
  • 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
  • thyroid disease
  • high blood pressure
  • diabetes
  • trouble urinating due to an enlarged prostate gland
  • liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

  • an allergic reaction to this product occurs. Seek medical help right away.
  • symptoms do not improve within 7 days or are accompanied by a fever
  • nervousness, dizziness or sleeplessness occurs

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 (1-800-222-1222).

Directions

adults and children 12 years and over1 tablet daily with a full glass of water; not more than 1 tablet in 24 hours
children under 12 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

Inactive ingredients

calcium carbonate, colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, sodium alginate, sodium citrate, talc and titanium dioxide

Questions?

call 1-800-406-7984

PRINCIPAL DISPLAY PANEL - 10 Tablet Blister Pack Carton

Compare to Claritin-D® 24 Hour active ingredients

NDC 37808-724-69

H-E-B®
Allergy Relief-D

Loratadine, USP 10 mg/Antihistamine
Pseudoephedrine Sulfate, USP 240 mg/Nasal Decongestant

Indoor & Outdoor Allergies

Non-Drowsy*

Allergy & Congestion
Original Prescription Strength

24
Hour

24 Hour Relief of:

10 EXTENDED-RELEASE TABLETS
*When taken as directed.See Drug Facts Panel.

actual
size

PRINCIPAL DISPLAY PANEL - 10 Tablet Blister Pack Carton
LORATADINE AND PSEUDOEPHEDRINE SULFATE 
loratadine and pseudoephedrine sulfate tablet, film coated, extended release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-724
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
loratadine (UNII: 7AJO3BO7QN) (loratadine - UNII:7AJO3BO7QN) loratadine10 mg
pseudoephedrine sulfate (UNII: Y9DL7QPE6B) (pseudoephedrine - UNII:7CUC9DDI9F) pseudoephedrine sulfate240 mg
Inactive Ingredients
Ingredient NameStrength
calcium carbonate (UNII: H0G9379FGK)  
silicon dioxide (UNII: ETJ7Z6XBU4)  
hydroxypropyl cellulose, unspecified (UNII: 9XZ8H6N6OH)  
hypromellose, unspecified (UNII: 3NXW29V3WO)  
ferrosoferric oxide (UNII: XM0M87F357)  
lactose monohydrate (UNII: EWQ57Q8I5X)  
magnesium stearate (UNII: 70097M6I30)  
microcrystalline cellulose (UNII: OP1R32D61U)  
polyethylene glycol, unspecified (UNII: 3WJQ0SDW1A)  
povidone, unspecified (UNII: FZ989GH94E)  
propylene glycol (UNII: 6DC9Q167V3)  
sodium alginate (UNII: C269C4G2ZQ)  
sodium citrate, unspecified form (UNII: 1Q73Q2JULR)  
talc (UNII: 7SEV7J4R1U)  
titanium dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorWHITE (White to Off-White) Scoreno score
ShapeCAPSULESize17mm
FlavorImprint Code RX724
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-724-6910 in 1 BLISTER PACK; Type 0: Not a Combination Product02/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07655702/01/2018
Labeler - HEB (007924756)

Revised: 4/2018
Document Id: 3e9fe73b-d3ee-4160-8dfa-8b099cd68e8a
Set id: 74e7670a-5eca-4556-a860-0d36e8561518
Version: 2
Effective Time: 20180412
 
HEB