Maximum Strength Antifungal Liquid
- Product NDC
- 81522-077
- 11-digit product format
- 815220077
- Labeler code
- 81522
- Product ID
- 81522-077_422aad2b-03e5-01e3-e063-6394a90adb31
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- FSA Store Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-04
- Substance
- TOLNAFTATE
- Active strength
- 10 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
- Maximum Strength Antifungal Liquid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81522-077-01 | Maximum Strength Antifungal Liquid | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | | 6 |
| 81522-077-01 | Maximum Strength Antifungal Liquid | 1 in 1 CARTON | LIQUID | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81522-077 | MAXIMUM STRENGTH ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [FSA STORE INC.] | 3 | Current NDC, 2 package rows | 20241109_fae36294-68b6-bf14-e053-6394a90aaacd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 81522-077-01 | 81522007701 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (81522-077-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR | 2023-05-04 | No | No | Historical |