daytime mucus relief severe congestion and cough and nighttime cold and flu maximum strength

Generic: dextromethorphan hbr, guaifenesin, phenylephrine hci, acetaminophen, diphenhydramine hci

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime mucus relief severe congestion and cough and nighttime cold and flu maximum strength
Generic Name dextromethorphan hbr, guaifenesin, phenylephrine hci, acetaminophen, diphenhydramine hci
Labeler walgreens
Dosage Form KIT
Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0862
Product ID 0363-0862_f8c61088-0340-4805-9d3c-8a711d9ca76f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2015-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630862
Hyphenated Format 0363-0862

Supplemental Identifiers

RxCUI
1043543 1375932 2637728
UPC
0311917177762

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 mucus relief severe congestion and cough and nighttime cold and flu maximum strength (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin, phenylephrine hci, acetaminophen, diphenhydramine hci (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 650 mg
  • 25 mg
  • 10 mg
  • 20 mg
  • 400 mg
source: label
Packaging
  • 1 KIT in 1 KIT (0363-0862-12) * 177 mL in 1 BOTTLE, PLASTIC (0363-0337-06) * 177 mL in 1 BOTTLE, PLASTIC (0363-0460-06)
source: ndc

Packages (1)

0363-0862-12 1 KIT in 1 KIT (0363-0862-12) * 177 mL in 1 BOTTLE, PLASTIC (0363-0337-06) * 177 mL in 1 BOTTLE, PLASTIC (0363-0460-06)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f8c61088-0340-4805-9d3c-8a711d9ca76f", "openfda": {"upc": ["0311917177762"], "rxcui": ["1043543", "1375932", "2637728"], "spl_set_id": ["366ddac8-9e8a-41bd-a7f7-48213485a5f8"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (0363-0862-12)  *  177 mL in 1 BOTTLE, PLASTIC (0363-0337-06)  *  177 mL in 1 BOTTLE, PLASTIC (0363-0460-06)", "package_ndc": "0363-0862-12", "marketing_start_date": "20150731"}], "brand_name": "Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum Strength", "product_id": "0363-0862_f8c61088-0340-4805-9d3c-8a711d9ca76f", "dosage_form": "KIT", "product_ndc": "0363-0862", "generic_name": "Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, Acetaminophen, Diphenhydramine HCI", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}