FUNGINIX AF
- Product NDC
- 71229-103
- 11-digit product format
- 712290103
- Labeler code
- 71229
- Product ID
- 71229-103_2f007d49-0eeb-511e-e063-6394a90ae3f8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- The Sisquoc Healthcare Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-25
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FUNGINIX AF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 103951 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71229-103-11 | FUNGINIX AF | 28 g in 1 TUBE | CREAM | 28 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71229-103 | FUNGINIX AF (TOLNAFTATE) CREAM [THE SISQUOC HEALTHCARE CORPORATION] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250227_f6cf5315-6678-486c-85b2-d4b3f748600e.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 |
|---|
| 71229-103-11 | 71229010311 | 28 g in 1 TUBE (71229-103-11) | 28 g | 2019-03-25 | 0000-00-00 | No | No | Current |