Home NDC 67172-150 Chloraseptic Nighttime Sore Throat Hot Relief
Product NDC 67172-150
11-digit product format 671720150
Labeler code 67172
Product ID 67172-150_726cdf80-c05c-4a6a-8d3e-a80f12f1acab
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen and diphenhydramine hydrochloride
Dosage form POWDER, FOR SOLUTION
Route ORAL
Labeler Prestige Brands Holdings, Inc.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-20
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 650; 25 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 Chloraseptic Nighttime Sore Throat Hot Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 650 mg/1 DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2670677 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 178 · 3,551 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 67172-150-06 67172015006 6 POWDER, FOR SOLUTION in 1 CARTON (67172-150-06) 2026-06-20 No No Current