Fungicure LiquidGel
- Product NDC
- 52389-633
- 11-digit product format
- 523890633
- Labeler code
- 52389
- Product ID
- 52389-633_7d3c822e-8c7b-5219-e053-2a91aa0abea8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Undecylenic Acid
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Alva-Amco Pharmacal Companies, Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-11-30
- Marketing end
- 0000-00-00
- Substance
- UNDECYLENIC ACID
- Active strength
- 250 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52389-633-09 | Fungicure LiquidGel | 1 in 1 BOX | GEL | 1 | | 9 |
| 52389-633-09 | Fungicure LiquidGel | 9 g in 1 TUBE, WITH APPLICATOR | GEL | 9 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52389-633 | FUNGICURE LIQUIDGEL (UNDECYLENIC ACID) GEL [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.] | 9 | Legacy NDC, 2 package rows | 20250110_ee5b4f26-0ed7-4e33-931e-8a31afa0cd9a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52389-633-09 | 52389063309 | 1 TUBE, WITH APPLICATOR in 1 BOX (52389-633-09) > 9 g in 1 TUBE, WITH APPLICATOR | 2016-06-05 | 0000-00-00 | No | No | Current |