Label: CORICIDIN HBP DAY AND NIGHT- dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate kit
- NDC Code(s): 11523-4111-1, 11523-4221-1, 11523-4765-1
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 30, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
-
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
- cough that occurs with excessive phlegm (mucus)
- persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema
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Directions
- do not exceed recommended dose
- do not take the Day and Night products at the same time; wait 4 hours after the last Night dose before starting Day product
- adults and children 12 years and over: 1 or 2 softgels every 4 hours, not more than 6 softgels in 12 hours
- children under 12 years of age: ask a doctor
- Other Information
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
-
Warnings
Liver Warning
This product contains acetaminophen.
Sever liver damage may occur if you take
- more than 4 tablets in 12 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
Do not use
- with any other drug containing acetaminophen (prescription or non prescription). 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 a MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
- liver disease
- glaucoma
- trouble urinating due to an enlarged prostate gland
- cough that occurs with excessive phlegm (mucus)
- a breathing problem or persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema
Ask a doctor or pharmacist before use if you are
- taking the blood thinning drug warfarin
- taking sedatives or tranquilizers
When using this product
- excitability may occur, especially in children
- marked drowsiness may occur
- avoid alcoholic beverages
- alcohol, sedatives and tranquilizers may increase drowsiness
- use caution when driving a motor vehicle or operating machinery
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Directions
- do not use more than directed (see overdose warning)
- do not take the Day and Night products at the same time; wait 4 hours after the last Day dose before starting Night product
- adults and children 12 years and over: 2 tablets at bedtime and every 6 hours if needed, while symptoms persist, not more than 4 tablets in a 12 hour period
- children under 12 years of age: ask a doctor
- Other Information
- Inactive Ingredients
- Questions or comments?
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PRINCIPAL DISPLAY PANEL - Kit Carton
DUAL FORMULA PACK
Coricidin ®
HBPDecongestant-free COLD RELIEF for people
with HIGH BLOOD PRESSUREDAY
MULTI-SYMPTOM COLD
Guaifenesin - Expectorant
Dextromethorphan HBr - Cough SuppressantDay Relieves:
- Chest Congestion
- Cough
16 DAY SOFTGELS
NIGHT
Chlorpheniramine Maleate - Antihistamine,
Dextromethorphan HBr - Cough Suppressant,
Acetaminophen - Pain Reliever/Fever ReducerSee New Warnings Information
Night Relieves:
- Runny Nose & Sneezing
- Cough • Body Aches
- Fever
8 NIGHT TABLETS
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INGREDIENTS AND APPEARANCE
CORICIDIN HBP DAY AND NIGHT
dextromethorphan hydrobromide, guaifenesin, acetaminophen, chlorpheniramine maleate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-4765 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-4765-1 1 in 1 CARTON; Type 0: Not a Combination Product 08/28/2009 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 BLISTER PACK 16 Part 2 2 BLISTER PACK 8 Part 1 of 2 CORICIDIN HBP DAY
dextromethorphan hydrobromide and guaifenesin capsule, gelatin coatedProduct Information Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GELATIN (UNII: 2G86QN327L) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POVIDONE (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) Product Characteristics Color red Score no score Shape OVAL Size 20mm Flavor Imprint Code C;DAY Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-4221-1 2 in 1 CARTON 1 8 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/28/2009 Part 2 of 2 CORICIDIN HBP NIGHT
acetaminophen, chlorpheniramine maleate and dextromethorphan hydrobromide tabletProduct Information Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 2 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) FD&C RED NO. 40 (UNII: WZB9127XOA) ALUMINUM OXIDE (UNII: LMI26O6933) HYPROMELLOSES (UNII: 3NXW29V3WO) LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POVIDONE (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color red Score no score Shape OVAL Size 18mm Flavor Imprint Code C;NIGHT Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-4111-1 2 in 1 CARTON 1 4 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/28/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/28/2009 Labeler - Bayer HealthCare LLC. (112117283)