Home NDC 85884-025 Cureforte Breath Reset
Product NDC 85884-025
11-digit product format 858840025
Labeler code 85884
Product ID 85884-025_3a6fc32c-9405-786c-e063-6394a90a83a9
Type HUMAN OTC DRUG
Nonproprietary name Mouth Spray
Dosage form SPRAY
Route ORAL
Labeler STEEL CITY HEALTH PRIVATE LIMITED
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-01
Substance CETYLPYRIDINIUM CHLORIDE; GLYCERIN
Active strength .85; 100 mg/mL; mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [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 Cureforte Breath Reset
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CETYLPYRIDINIUM CHLORIDE .85 mg/mL GLYCERIN 100 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination D9OM4SK49P Internal UNII lookup PDC6A3C0OX Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85884-025-01 Cureforte Breath Reset 35 mL in 1 BOTTLE, SPRAY SPRAY 35 2
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 24 of 40 · 786 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85884-025-01 85884002501 35 mL in 1 BOTTLE, SPRAY (85884-025-01) 35 ml 2025-08-01 No No Current