up and up daytime nighttime childrens multi symptom cold

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

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

Drug Facts

Product Profile

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

Identifiers & Regulatory

Product NDC 82442-476
Product ID 82442-476_440646d8-f515-5968-e063-6394a90ab7cd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82442476
Hyphenated Format 82442-476

Supplemental Identifiers

RxCUI
1043543 1375932 2637728

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 nighttime childrens multi symptom cold (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, diphenhydramine hydrochloride, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 5 ml
  • 5 mg
  • 100 mg
  • 2.5 mg
  • 10 ml
  • 325 mg
  • 12.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (82442-476-08) * 118 mL in 1 BOTTLE (82442-469-04) * 118 mL in 1 BOTTLE (82442-377-04)
source: ndc

Packages (1)

82442-476-08 1 KIT in 1 CARTON (82442-476-08) * 118 mL in 1 BOTTLE (82442-469-04) * 118 mL in 1 BOTTLE (82442-377-04)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

up and up Daytime Nighttime Childrens Multi Symptom Cold ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "440646d8-f515-5968-e063-6394a90ab7cd", "openfda": {"rxcui": ["1043543", "1375932", "2637728"], "spl_set_id": ["b8a4da0b-e4d3-48e6-b699-cb56c7b67ed7"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (82442-476-08)  *  118 mL in 1 BOTTLE (82442-469-04)  *  118 mL in 1 BOTTLE (82442-377-04)", "package_ndc": "82442-476-08", "marketing_start_date": "20240719"}], "brand_name": "up and up Daytime Nighttime Childrens Multi Symptom Cold", "product_id": "82442-476_440646d8-f515-5968-e063-6394a90ab7cd", "dosage_form": "KIT", "product_ndc": "82442-476", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up Daytime Nighttime Childrens Multi Symptom Cold", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240719", "listing_expiration_date": "20261231"}