NDC 0280-1570

Alka-Seltzer Plus Maximum Strength Cold and Cough

Acetaminophen, Chlorpheniramine Malaeate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride

Alka-Seltzer Plus Maximum Strength Cold and Cough is a Oral Capsule, Liquid Filled in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Chlorpheniramine Maleate; Phenylephrine Hydrochloride; Dextromethorphan Hydrobromide; Acetaminophen.

• Product ID: 0280-1570_715ea87c-0df5-4810-e053-2995a90a01de
• NDC: 0280-1570
• Product Type: Human Otc Drug
• Proprietary Name: Alka-Seltzer Plus Maximum Strength Cold and Cough
• Generic Name: Acetaminophen, Chlorpheniramine Malaeate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
• Dosage Form: Capsule, Liquid Filled
• Route of Administration: ORAL
• Marketing Start Date: 2017-06-16
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Bayer HealthCare LLC.
• Substance Name: CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN
• Active Ingredient Strength: 2 mg/1; mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0280-1570-10

1 BLISTER PACK in 1 CARTON (0280-1570-10) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

• Marketing Start Date: 2017-06-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0280-1570-10 [00280157010]

Alka-Seltzer Plus Maximum Strength Cold and Cough CAPSULE, LIQUID FILLED

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-16

NDC 0280-1570-20 [00280157020]

Alka-Seltzer Plus Maximum Strength Cold and Cough CAPSULE, LIQUID FILLED

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-16

NDC 0280-1570-40 [00280157040]

Alka-Seltzer Plus Maximum Strength Cold and Cough CAPSULE, LIQUID FILLED

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-06-16

Drug Details

Active Ingredients

Ingredient	Strength
CHLORPHENIRAMINE MALEATE	2 mg/1

OpenFDA Data

• SPL SET ID: 51dec468-fbb2-3489-e054-00144ff88e88
• Manufacturer:
  • Bayer HealthCare LLC.
• UNII:
  • V1Q0O9OJ9Z
  • 362O9ITL9D
  • 04JA59TNSJ
  • 9D2RTI9KYH
• RxNorm Concept Unique ID - RxCUI:
  • 1042688
• UPC Code:
  • 0016500555346

NDC Crossover Matching brand name "Alka-Seltzer Plus Maximum Strength Cold and Cough" or generic name "Acetaminophen, Chlorpheniramine Malaeate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride"

NDC	Brand Name	Generic Name
0280-1212	Alka-Seltzer Plus Maximum Strength Cold and Cough	Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, Phenylephrine hydrochloride
0280-1570	Alka-Seltzer Plus Maximum Strength Cold and Cough	Acetaminophen, Chlorpheniramine malaeate, Dextromethorphan hydrobromide, Phenylephrine hydrochloride
0280-0092	Alka-Seltzer Plus Maximum Strength Cold and Cough Power Max Gels	Acetaminophen, Chlorpheniramine malaeate, Dextromethorphan hydrobromide, Phenylephrine hydrochloride