Package 50580-529-01

Brand: tylenol cold plus flu severe day and tylenol cold plus flu plus cough night 3-pack

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and guaifenesin, phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-529-01
Digits Only 5058052901
Product NDC 50580-529
Product ID 50580-529_22c8b85f-d4e8-f3d7-e063-6394a90ae316
Description

1 KIT in 1 PACKAGE (50580-529-01) * 240 mL in 1 BOTTLE (50580-369-01) * 240 mL in 1 BOTTLE, PLASTIC (50580-403-08)

Marketing

Marketing Status
Marketed Since 2019-08-05
Brand tylenol cold plus flu severe day and tylenol cold plus flu plus cough night 3-pack
Generic acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and guaifenesin, phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "22c8b85f-d4e8-f3d7-e063-6394a90ae316", "openfda": {"upc": ["0300450562081", "0300450525086"], "rxcui": ["1369842", "1431245", "2637731"], "spl_set_id": ["464de5de-0e7a-41d6-875f-dd0e5fe7893c"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE (50580-529-01)  *  240 mL in 1 BOTTLE (50580-369-01)  *  240 mL in 1 BOTTLE, PLASTIC (50580-403-08)", "package_ndc": "50580-529-01", "marketing_start_date": "20190805"}], "brand_name": "Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack", "product_id": "50580-529_22c8b85f-d4e8-f3d7-e063-6394a90ae316", "dosage_form": "KIT", "product_ndc": "50580-529", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and guaifenesin, phenylephrine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190805", "listing_expiration_date": "20261231"}