Package 69842-800-40

Brand: nighttime severe

Generic: acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 69842-800-40
Digits Only 6984280040
Product NDC 69842-800
Product ID 69842-800_6eb654a8-b00d-4174-988d-407ee9b74361
Description

355 mL in 1 BOTTLE (69842-800-40)

Marketing

Marketing Status
Marketed Since 2016-06-23
Brand nighttime severe
Generic acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Nighttime Severe ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6eb654a8-b00d-4174-988d-407ee9b74361", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2", "04JA59TNSJ"], "rxcui": ["1431245"], "spl_set_id": ["43784616-1afd-4ff7-8fee-6ac389f616a2"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (69842-800-40)", "package_ndc": "69842-800-40", "marketing_start_date": "20160623"}], "brand_name": "Nighttime Severe", "product_id": "69842-800_6eb654a8-b00d-4174-988d-407ee9b74361", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "69842-800", "generic_name": "Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nighttime Severe", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "12.5 mg/30mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160623", "listing_expiration_date": "20261231"}