NDC 50580-414

TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT

Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride

TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT is a Kit in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is .

• Product ID: 50580-414_504e3e04-612b-4470-9767-65a2bbd79562
• NDC: 50580-414
• Product Type: Human Otc Drug
• Proprietary Name: TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT
• Generic Name: Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride
• Dosage Form: Kit
• Marketing Start Date: 2016-07-18
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 50580-414-03

3 CARTON in 1 CELLO PACK (50580-414-03) > 1 KIT in 1 CARTON (50580-414-01) * 4 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2016-07-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50580-414-03 [50580041403]

TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT KIT

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-07-18

NDC 50580-414-04 [50580041404]

TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT KIT

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-12-21

NDC 50580-414-01 [50580041401]

TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT KIT

• Marketing Category: OTC monograph final
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-07-18

Drug Details

OpenFDA Data

• SPL SET ID: 2ddb86a8-e34c-4a03-a60a-d3fedaf90608
• Manufacturer:
  • Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
• RxNorm Concept Unique ID - RxCUI:
  • 1110988
  • 1801964
  • 1086991

NDC Crossover Matching brand name "TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT" or generic name "Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride"

NDC	Brand Name	Generic Name
50580-414	TYLENOL COLD PLUS FLU SEVERE DAY/NIGHT	acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
53943-186	COLD AND FLU SEVERE	Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
63868-238	Cold and Flu Severe Daytime and Nighttime	Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
41250-753	cold and flu severe daytime nighttime	Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
37808-286	Cold Flu Severe Day Night	Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
72036-186	Cold Flu Severe Day Night	Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride