Home NDC 67751-217 Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz
Product NDC 67751-217
11-digit product format 677510217
Labeler code 67751
Product ID 67751-217_2395eed2-0bab-a839-e063-6394a90aded6
Type HUMAN OTC DRUG
Nonproprietary name chlorpheniramine maleate, acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler Navajo Manufacturing Company Inc.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-01
Substance DEXTROMETHORPHAN HYDROBROMIDE; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN
Active strength 10; 2; 5; 250 mg/1; mg/1; mg/1; mg/1
Pharmacologic 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]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 CHLORPHENIRAMINE MALEATE 2 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1 ACETAMINOPHEN 250 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1536477 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67751-217-01 Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 1 in 1 CARTON TABLET, EFFERVESCENT 1 2 67751-217-01 Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 1 in 1 POUCH TABLET, EFFERVESCENT 1 2 67751-217-02 Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 2 in 1 POUCH TABLET, EFFERVESCENT 2 2 67751-217-02 Alka-Seltzer Plus Severe Cold and Flu PowerFast Fizz 1 in 1 CARTON TABLET, EFFERVESCENT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67751-217 ALKA-SELTZER PLUS SEVERE COLD AND FLU POWERFAST FIZZ (CHLORPHENIRAMINE MALEATE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE) TABLET, EFFERVESCENT [NAVAJO MANUFACTURING COMPANY INC.] 2 Current NDC, 4 package rows 20241004_f6068011-ad56-59b4-e053-2995a90ac016.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 98 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 67751-217-01 67751021701 1 POUCH in 1 CARTON (67751-217-01) / 1 TABLET, EFFERVESCENT in 1 POUCH 1 pouch 2022-06-01 No No Current 67751-217-02 67751021702 1 POUCH in 1 CARTON (67751-217-02) / 2 TABLET, EFFERVESCENT in 1 POUCH 1 pouch 2022-06-01 No No Current