Package 11673-877-55

Brand: up and up daytime multi symptom severe cold nighttime severe cold and cough

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11673-877-55
Digits Only 1167387755
Product NDC 11673-877
Product ID 11673-877_17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b
Description

1 KIT in 1 CARTON (11673-877-55) * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-122-00) * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-964-00)

Marketing

Marketing Status
Discontinued 2026-08-01
Brand up and up daytime multi symptom severe cold nighttime severe cold and cough
Generic acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b", "openfda": {"rxcui": ["1189316", "1659960", "2640034"], "spl_set_id": ["50ecad33-a2b1-483e-9f03-000caa2af91c"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11673-877-55)  *  1 POWDER, FOR SOLUTION in 1 PACKET (82442-122-00)  *  1 POWDER, FOR SOLUTION in 1 PACKET (82442-964-00)", "package_ndc": "11673-877-55", "marketing_end_date": "20260801", "marketing_start_date": "20210716"}], "brand_name": "Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough", "product_id": "11673-877_17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b", "dosage_form": "KIT", "product_ndc": "11673-877", "generic_name": "acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260801", "marketing_start_date": "20210716"}