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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cureforte Breath Reset
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CETYLPYRIDINIUM CHLORIDE | .85 mg/mL |
| GLYCERIN | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | D9OM4SK49P, PDC6A3C0OX |
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 |
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 |