Label: NOREL AD- Acetaminophen, Chlorpheniramine Maleate, And ...
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- NDC Code(s): 52747-475-70
- Packager: U.S. PHARMACEUTICAL CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
- nasal congestion
- runny nose
- minor aches and pains
- headache
- sore throat
- sneezing
- itchy, watery eyes
- itching of the nose or throat
- sinus congestion and pressure
- temporarily reduces fever
- Warnings
Liver warning:This product contains acetaminophen. Severe liver damage may occur if
- adult takes more than 6 tablets in 24 hours, which is the maximum daily amount
- child takes more than 5 doses in 24 hours
- taken with other drugs containing acetaminophen
- adult has 3 or more alcoholic drinks every day while using this product
Allergy 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, speak with a healthcare provider.
- Do not use
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- 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
- liver disease
- heart disease
- high blood pressure
- thyroid disease
- diabetes
- glaucoma
- trouble urinating due to an enlarged prostate gland
- a breathing problem such as emphysema or chronic bronchitis
- Ask a doctor or pharmacist before use if you are
- taking the blood thinning drug warfarin
- taking any other nasal decongestant or stimulant
- taking sedatives or tranquilizers
- When using this product
- do not exceed recommended dosage
- drowsiness may occur
- avoid alcoholic beverages
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
- excitability may occur, especially in children
- Stop use and ask a doctor if
- pain or nasal congestion gets worse or lasts more than 7 days
- fever gets worse or lasts more than 3 days
- redness or swelling is present
- you get nervous, dizzy, or sleepless
- new symptoms occur
- If pregnant or breast feeding
- ask a health professional before use
- 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
- do not take more than directed (see overdose warning)
- adults and children 12 years of age and over: take 1 tablet every 4 hours, while symptoms persist
- do not take more than 6 tablets in 24 hours, unless directed by a doctor
- children under 12 years of age: ask a doctor
- 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
- INGREDIENTS AND APPEARANCE
NOREL AD acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52747-475 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 4 mg PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength 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 Color yellow, white Score no score Shape TRIANGLE (Arc) Size 11mm Flavor Imprint Code 0425;US Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52747-475-70 20 in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/27/2012 Labeler - U.S. PHARMACEUTICAL CORPORATION (079467662)
Find additional resources
(also available in the left menu)Safety
Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk
Related Resources
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More Info on this Drug
View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!
NOREL AD- acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer
Number of versions: 13
| Published Date (What is this?) | Version | Files |
|---|---|---|
| Nov 17, 2025 | 14 (current) | download |
| Oct 17, 2024 | 13 | download |
| Oct 13, 2023 | 12 | download |
| Nov 30, 2022 | 11 | download |
| Nov 21, 2022 | 10 | download |
| Oct 12, 2021 | 9 | download |
| Nov 18, 2020 | 8 | download |
| Nov 15, 2019 | 7 | download |
| Nov 9, 2017 | 6 | download |
| Oct 1, 2014 | 5 | download |
| Jun 20, 2013 | 3 | download |
| Aug 30, 2012 | 2 | download |
| Apr 30, 2012 | 1 | download |
NOREL AD- acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer
| RxCUI | RxNorm NAME | RxTTY | |
|---|---|---|---|
| 1 | 1193293 | acetaminophen 325 MG / chlorpheniramine maleate 4 MG / phenylephrine HCl 10 MG Oral Tablet | PSN |
| 2 | 1193293 | acetaminophen 325 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 MG Oral Tablet | SCD |
| 3 | 1193293 | APAP 325 MG / chlorpheniramine maleate 4 MG / phenylephrine hydrochloride 10 MG Oral Tablet | SY |
NOREL AD- acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer
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NOREL AD- acetaminophen, chlorpheniramine maleate, and phenylephrine hcl tablet, multilayer
If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.
| NDC | |
|---|---|
| 1 | 52747-475-70 |
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