FLUSH Maximum Strength Antifungal formula
- Product NDC
- 80569-084
- 11-digit product format
- 805690084
- Labeler code
- 80569
- Product ID
- 80569-084_09e240de-0009-c20f-e063-6294a90a09c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- UNDECYLENIC ACID
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Triple Point Group, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-17
- Substance
- UNDECYLENIC ACID
- Active strength
- 250 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FLUSH Maximum Strength Antifungal formula
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| UNDECYLENIC ACID | 250 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K3D86KJ24N |
| Rxcui | 998329 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80569-084-15 | FLUSH Maximum Strength Antifungal formula | 15 mL in 1 BOTTLE, GLASS | LIQUID | 15 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80569-084 | FLUSH MAXIMUM STRENGTH ANTIFUNGAL FORMULA (UNDECYLENIC ACID) LIQUID [TRIPLE POINT GROUP, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231112_1d9e56ef-c7c9-4aff-ab9e-b163e566e3d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80569-084-15 | 80569008415 | 15 mL in 1 BOTTLE, GLASS (80569-084-15) | 15 ml | 2020-09-17 | 0000-00-00 | No | No | Current |