Flexitol Medicated Foot
- Product NDC
- 43251-3340
- 11-digit product format
- 432513340
- Labeler code
- 43251
- Product ID
- 43251-3340_32d36fb9-913b-4581-a2af-dc45211a4a4b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LaCorium Health International Pty Ltd
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-08-11
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43251-3340-1 | Flexitol Medicated Foot | 1 in 1 CARTON | CREAM | 1 | | 1 |
| 43251-3340-1 | Flexitol Medicated Foot | 56 g in 1 TUBE | CREAM | 56 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43251-3340 | FLEXITOL MEDICATED FOOT (TOLNAFTATE) CREAM [LACORIUM HEALTH INTERNATIONAL PTY LTD] | 1 | Legacy NDC, 2 package rows | 20121121_c31da255-e671-41e3-8607-efbb6973163c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 43251-3340-1 | 43251334001 | 1 in 1 CARTON | Historical |