Natralia Anti Fungal
- Product NDC
- 43251-3361
- 11-digit product format
- 432513361
- Labeler code
- 43251
- Product ID
- 43251-3361_199871d6-9fc1-477d-9bb4-9b42794b0f70
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Undecylenic acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Lacorium Health USA Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-01-03
- Marketing end
- 2022-05-31
- Substance
- UNDECYLENIC ACID
- Active strength
- 250 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43251-3361-1 | 43251336101 | 1 BOTTLE in 1 CARTON (43251-3361-1) > 30 mL in 1 BOTTLE | 1 bottle | 2009-01-03 | 2022-05-31 | No | No | Current |