NOREL AD- acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer 
U.S. PHARMACEUTICAL CORPORATION

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Norel® AD

Drug Facts

Active Ingredients (per tablet)

Acetaminophen 325 mg

Chlorpheniramine Maleate 4 mg

Phenylephrine HCl 10 mg

Purpose

Pain reliever

Antihistamine

Nasal decongestant

Uses

Temporarily relieves these symptoms due to the common cold or flu

Warnings

Liver warning:This product contains acetaminophen. Severe liver damage may occur if

Allergy alert:Acetaminophen may cause severe skin reaction.
Symptoms may include:

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, speak with a healthcare provider.

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

Keep out of the reach of children.

Taking more than the recommended dose can cause serious health problems. In case of overdose, get medical help or contact 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

Other Information

store at 20°-25°C (68°-77°F)

Overdose Warning:Keep this and all medication out of the reach of children. In case of accidental overdose, seek medical help or contact a Poison Control Center immediately.

Inactive Ingredients

Colloidal Silicon Dioxide, Crospovidone Polyplasdone, Magnesium Stearate (vegetable base), Microcrystalline Cellulose, Povidone K-30, Pregelatinized Starch, Stearic Acid, D&C Yellow #10, FD&C Yellow #6.

Questions or Comments

Please visit www.uspco.comor contact us at US Pharmaceutical Corporation, P.O. Box 360465, Decatur, GA 30036

Principal Display Panel

Figure 1:Norel ®AD container label

Norel AD container label
NOREL AD 
acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52747-475
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POVIDONE K30 (UNII: U725QWY32X)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Product Characteristics
Coloryellow, whiteScoreno score
ShapeTRIANGLE (Arc) Size11mm
FlavorImprint Code 0425;US
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52747-475-7020 in 1 BOTTLE; Type 0: Not a Combination Product04/27/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/27/2012
Labeler - U.S. PHARMACEUTICAL CORPORATION (079467662)

Revised: 10/2023
Document Id: 078bb582-0cfe-3dea-e063-6394a90a8604
Set id: 53d9ed3c-212d-4b12-ac35-8bd49382b49d
Version: 12
Effective Time: 20231012
 
U.S. PHARMACEUTICAL CORPORATION