alka-seltzer plus severe cold and flu powerfast fizz

Generic: chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide

Labeler: r j general corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alka-seltzer plus severe cold and flu powerfast fizz
Generic Name chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide
Labeler r j general corporation
Dosage Form TABLET, EFFERVESCENT
Routes
ORAL
Active Ingredients

acetaminophen 250 mg/1, chlorpheniramine maleate 2 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
R J General Corporation

Identifiers & Regulatory

Product NDC 70264-016
Product ID 70264-016_43c89da9-1ee5-db2f-e063-6394a90a9248
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-03-16

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] 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 70264016
Hyphenated Format 70264-016

Supplemental Identifiers

RxCUI
1536477
UNII
362O9ITL9D V1Q0O9OJ9Z 9D2RTI9KYH 04JA59TNSJ

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 alka-seltzer plus severe cold and flu powerfast fizz (source: ndc)
Generic Name chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 2 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (70264-016-01) / 2 TABLET, EFFERVESCENT in 1 POUCH
source: ndc

Packages (1)

70264-016-01 30 POUCH in 1 CARTON (70264-016-01) / 2 TABLET, EFFERVESCENT in 1 POUCH

Ingredients (4)

acetaminophen (250 mg/1) chlorpheniramine maleate (2 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c89da9-1ee5-db2f-e063-6394a90a9248", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1536477"], "spl_set_id": ["d786ae07-ce57-44c7-9ba5-f4c87df115de"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (70264-016-01)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "70264-016-01", "marketing_start_date": "20230316"}], "brand_name": "Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz", "product_id": "70264-016_43c89da9-1ee5-db2f-e063-6394a90a9248", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "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": "70264-016", "generic_name": "chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "2 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": "20230316", "listing_expiration_date": "20261231"}