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 17 of 40 · 786 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join WALMART SALINE SALINE NASAL (SODIUM CHLORIDE) WALMART STORES INC 06906744-49a5-4bab-8539-af2d235df9e8 2025-10-28 Warnings Exact identifier application number: M022 Saline NASAL PUBLIX SUPER MARKETS, INC 19841567-9511-43d6-ba4e-d1e1bd3481a4 2025-10-28 Warnings Exact identifier application number: M022 PUBLIX Sore Throat Fast Relief Oral Anesthetic PHENOL PUBLIX SUPER MARKETS, INC 89291f12-bbc3-4472-8ad3-a34485af72c9 2025-10-28 Warnings Exact identifier application number: M022 PUBLIX Sore Throat Menthol Flavor PHENOL PUBLIX SUPER MARKETS, INC 9296c49e-557c-43ed-9527-fcba5093a8dc 2025-10-28 Warnings Exact identifier application number: M022 WinCo Foods Maximum Strength Oral Analgesic BENZOCAINE WinCo Foods, LLC c22a7726-8c3f-41bf-b852-8456b2be6f93 2025-10-28 Warnings Exact identifier application number: M022 Rugby Cherry Flavor PHENOL RUGBY LABORATORIES 3d668c78-8130-45d4-bcb7-dddcb2fbe7a3 2025-10-25 Warnings Exact identifier application number: M022 LolliCaine Bubble Gum BENZOCAINE Centrix, Inc. 56ae3a84-6bca-4906-a03d-9d755e1fba3b 2025-10-24 Warnings Exact identifier application number: M022 Diabetic Tussin Sore Throat Cherry PHENOL MEDTECH PRODUCTS INC ab351229-5771-4c6c-92a8-721cc41c002f 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Total Sore Throat and Cough, Sugar Free MENTHOL AND BENZOCAINE AND DEXTROMETHORPHAN HYDROBROMIDE Prestige Brands Holdings, Inc. 34e4234c-ed61-4795-99fe-d281cdb0af88 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Total Sore Throat and Cough MENTHOL AND BENZOCAINE AND DEXTROMETHORPHAN HYDROBROMIDE Prestige Brands Holdings, Inc. 6b1a50d0-be54-4fcb-b5e2-b47abf3555c0 2025-10-23 Warnings Exact identifier application number: M022 Chloraseptic Childrens Sore Throat Cherry PHENOL Prestige Brands Holdings, Inc. 38ff6922-1abe-4fa9-a74e-ede604f707b5 2025-10-23 Warnings Exact identifier application number: M022 Boka Sensitive POTASSIUM NITRATE Karaka LLC 40be9fab-53db-c67a-e063-6394a90a48cb 2025-10-23 Warnings Exact identifier application number: M022 Canker Care Plus MENTHOL, UNSPECIFIED FORM Quantum, Inc. 1ec960db-52d5-4d99-a7f7-a2e538d28724 2025-10-20 Warnings Exact identifier application number: M022 meijer Sensitive EXTRA WHITENING POTASSIUM NITRATE, SODIUM FLUORIDE Meijer, Inc. bbcffb88-0bd4-4883-bb83-0b7a1428ad12 2025-10-20 Warnings Exact identifier application number: M022 Quality Choice Maximum Strength Oral Pain Relieving BENZOCAINE Chain Drug Marketing Association Inc dbde8e7f-85d8-4083-b01a-3a7e410a7747 2025-10-17 Warnings Exact identifier application number: M022 Quality Choice BENZOCAINE Chain Drug Marketing Association, Inc. 24c3c4a3-bd76-198d-e063-6394a90ad45a 2025-10-16 Warnings Exact identifier application number: M022 Sore Throat Relief Cherry Flavor PHENOL Cardinal Health b84203bd-23e9-427d-83d8-f4c88266e23c 2025-10-14 Warnings Exact identifier application number: M022 Finafta BENZOCAINE, GLYCERIN Efficient Laboratories Inc. 03368603-3e11-c2fa-e063-6294a90a04ea 2025-10-14 Warnings Exact identifier application number: M022 Sensodyne Pronamel Clinical Enamel Strength Whitening Action POTASSIUM NITRATE, SODIUM FLUORIDE Haleon US Holdings LLC e8a62f24-1db6-45fb-b6e1-5e57103f82bc 2025-10-14 Warnings Exact identifier application number: M022 evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT POTASSIUM NITRATE, SODIUM FLUORIDE Ashtel Studios, Inc. bc74d2a6-fe34-44cf-b015-70ed4d47c933 2025-10-13 Warnings Exact identifier application number: M022
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