maximum strength daytime cold and flu and nighttime severe cold and flu

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

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

Drug Facts

Product Profile

Brand Name maximum strength daytime cold and flu and nighttime severe cold and flu
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride,triprolidine hydrochloride
Labeler target corporation
Dosage Form KIT
Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-286
Product ID 11673-286_203f3d03-46d9-3747-e063-6294a90a251e
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 11673286
Hyphenated Format 11673-286

Supplemental Identifiers

RxCUI
1116572 2173662 2637727
UPC
0311673286012

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 maximum strength daytime cold and flu and nighttime severe cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride,triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 650 mg
  • 20 mg
  • 400 mg
  • 10 mg
  • 2.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (11673-286-01) * 180 mL in 1 BOTTLE (11673-872-03) * 180 mL in 1 BOTTLE (11673-295-03)
source: ndc

Packages (1)

11673-286-01 1 KIT in 1 CARTON (11673-286-01) * 180 mL in 1 BOTTLE (11673-872-03) * 180 mL in 1 BOTTLE (11673-295-03)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "203f3d03-46d9-3747-e063-6294a90a251e", "openfda": {"upc": ["0311673286012"], "rxcui": ["1116572", "2173662", "2637727"], "spl_set_id": ["0fc523ce-55a7-6384-e063-6394a90aad3f"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11673-286-01)  *  180 mL in 1 BOTTLE (11673-872-03)  *  180 mL in 1 BOTTLE (11673-295-03)", "package_ndc": "11673-286-01", "marketing_start_date": "20240501"}], "brand_name": "Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu", "product_id": "11673-286_203f3d03-46d9-3747-e063-6294a90a251e", "dosage_form": "KIT", "product_ndc": "11673-286", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, and Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride,Triprolidine Hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}