Package 63824-115-66

Brand: maximum strength mucinex sinus-max severe congestion and pain and mucinex nightshift sinus

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

Package Facts

Identity

Package NDC 63824-115-66
Digits Only 6382411566
Product NDC 63824-115
Product ID 63824-115_29940c89-5dc4-bf24-e063-6394a90a5c7a
Description

1 KIT in 1 CARTON (63824-115-66) * 180 mL in 1 BOTTLE (63824-266-66) * 180 mL in 1 BOTTLE (63824-269-66)

Marketing

Marketing Status
Marketed Since 2022-05-30
Brand maximum strength mucinex sinus-max severe congestion and pain and mucinex nightshift sinus
Generic acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Maximum Strength Mucinex Sinus-Max Severe Congestion and Pain and Mucinex Nightshift Sinus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "29940c89-5dc4-bf24-e063-6394a90a5c7a", "openfda": {"rxcui": ["1116568", "2173662", "2397132"], "spl_set_id": ["75c6b92f-219f-4740-bb72-c02a927a21ff"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (63824-115-66)  *  180 mL in 1 BOTTLE (63824-266-66)  *  180 mL in 1 BOTTLE (63824-269-66)", "package_ndc": "63824-115-66", "marketing_start_date": "20220530"}], "brand_name": "Maximum Strength Mucinex Sinus-Max Severe Congestion and Pain and Mucinex Nightshift Sinus", "product_id": "63824-115_29940c89-5dc4-bf24-e063-6394a90a5c7a", "dosage_form": "KIT", "product_ndc": "63824-115", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Mucinex Sinus-Max Severe Congestion and Pain and Mucinex Nightshift Sinus", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220530", "listing_expiration_date": "20261231"}