daytime nighttime ultra concentrated cold and flu

Generic: daytime - acetaminophen, dextromethrophan hbr, phenylephrine hcl and nighttime - acetaminophen, dextromethrophan hbr, doxylamine succinate

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

Drug Facts

Product Profile

Brand Name daytime nighttime ultra concentrated cold and flu
Generic Name daytime - acetaminophen, dextromethrophan hbr, phenylephrine hcl and nighttime - acetaminophen, dextromethrophan hbr, doxylamine succinate
Labeler target corporation
Dosage Form KIT
Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-848
Product ID 11673-848_203eb1d0-928c-0559-e063-6394a90a0fb8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673848
Hyphenated Format 11673-848

Supplemental Identifiers

RxCUI
1086997 1426334 1648203
UPC
0311673848838

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 daytime nighttime ultra concentrated cold and flu (source: ndc)
Generic Name daytime - acetaminophen, dextromethrophan hbr, phenylephrine hcl and nighttime - acetaminophen, dextromethrophan hbr, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (11673-848-83) * 48 CAPSULE, LIQUID FILLED in 1 BOTTLE * 48 CAPSULE, LIQUID FILLED in 1 BOTTLE
source: ndc

Packages (1)

11673-848-83 1 KIT in 1 CARTON (11673-848-83) * 48 CAPSULE, LIQUID FILLED in 1 BOTTLE * 48 CAPSULE, LIQUID FILLED in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Nighttime Ultra Concentrated Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "203eb1d0-928c-0559-e063-6394a90a0fb8", "openfda": {"upc": ["0311673848838"], "rxcui": ["1086997", "1426334", "1648203"], "spl_set_id": ["0c0cf76f-2dd3-45ef-e063-6394a90a9fef"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11673-848-83)  *  48 CAPSULE, LIQUID FILLED in 1 BOTTLE *  48 CAPSULE, LIQUID FILLED in 1 BOTTLE", "package_ndc": "11673-848-83", "marketing_start_date": "20240501"}], "brand_name": "Daytime Nighttime Ultra Concentrated Cold and Flu", "product_id": "11673-848_203eb1d0-928c-0559-e063-6394a90a0fb8", "dosage_form": "KIT", "product_ndc": "11673-848", "generic_name": "Daytime - Acetaminophen, Dextromethrophan HBr, Phenylephrine HCL and Nighttime - Acetaminophen, Dextromethrophan HBr, Doxylamine succinate", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Nighttime", "brand_name_suffix": "Ultra Concentrated Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}