maximum strenght day cold and flu formula

Generic: acetaminophen, dextromethorphan, phenylephrine hcl

Labeler: family dollar
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strenght day cold and flu formula
Generic Name acetaminophen, dextromethorphan, phenylephrine hcl
Labeler family dollar
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
FAMILY DOLLAR

Identifiers & Regulatory

Product NDC 55319-933
Product ID 55319-933_2e2d13f2-9446-dd98-e063-6394a90a9abb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-08-05

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55319933
Hyphenated Format 55319-933

Supplemental Identifiers

RxCUI
1086997
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

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 strenght day cold and flu formula (source: ndc)
Generic Name acetaminophen, dextromethorphan, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (55319-933-22)
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e2d13f2-9446-dd98-e063-6394a90a9abb", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["aa8ebccf-6813-2dca-e053-2a95a90a032b"], "manufacturer_name": ["FAMILY DOLLAR"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (55319-933-22)", "package_ndc": "55319-933-22", "marketing_start_date": "20200805"}], "brand_name": "MAXIMUM STRENGHT DAY COLD AND FLU FORMULA", "product_id": "55319-933_2e2d13f2-9446-dd98-e063-6394a90a9abb", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55319-933", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL", "labeler_name": "FAMILY DOLLAR", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGHT DAY COLD AND FLU FORMULA", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200805", "listing_expiration_date": "20261231"}