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

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

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name up and up daytime multi symptom severe cold nighttime severe cold and cough
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride
Labeler target corporation
Dosage Form KIT
Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-877
Product ID 11673-877_17b7ffd1-5422-4b0e-9fec-e7e93fe97f4b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2021-07-16
Marketing End 2026-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673877
Hyphenated Format 11673-877

Supplemental Identifiers

RxCUI
1189316 1659960 2640034

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name up and up daytime multi symptom severe cold nighttime severe cold and cough (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 500 mg
  • 20 mg
  • 10 mg
  • 650 mg
  • 25 mg
source: label
Packaging
  • 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)
source: ndc

Packages (1)

11673-877-55 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)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough ndc-match (0.9)

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"}