Package 69842-882-09

Brand: sinus relief daytime, nighttime, maximum strength

Generic: acetaminophen, diphenhydramine hcl, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 69842-882-09
Digits Only 6984288209
Product NDC 69842-882
Description

1 KIT in 1 CARTON (69842-882-09) * 10 TABLET, FILM COATED in 1 BLISTER PACK * 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-07-01
Brand sinus relief daytime, nighttime, maximum strength
Generic acetaminophen, diphenhydramine hcl, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "523977ae-9c49-4699-8c95-24efba4a09b7", "openfda": {"rxcui": ["1233575", "1243679", "2634398"], "spl_set_id": ["f6b3ca40-7638-477f-b800-4c28c40ff0a8"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (69842-882-09)  *  10 TABLET, FILM COATED in 1 BLISTER PACK *  10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "69842-882-09", "marketing_start_date": "20170701"}], "brand_name": "Sinus Relief Daytime, Nighttime, Maximum Strength", "product_id": "69842-882_523977ae-9c49-4699-8c95-24efba4a09b7", "dosage_form": "KIT", "product_ndc": "69842-882", "generic_name": "Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Relief", "brand_name_suffix": "Daytime, Nighttime, Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170701", "listing_expiration_date": "20261231"}