Antifungal Solution Maximum Strength
- Product NDC
- 11822-9600
- 11-digit product format
- 118229600
- Labeler code
- 11822
- Product ID
- 11822-9600_380fec4c-2ab4-ac75-e063-6294a90a0d57
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Rite Aid Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-12
- Marketing end
- 2026-09-30
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antifungal Solution Maximum Strength
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 |
|---|
| 11822-9600-1 | Antifungal Solution Maximum Strength | 1 in 1 CARTON | LIQUID | 1 | | 4 |
| 11822-9600-1 | Antifungal Solution Maximum Strength | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-9600 | ANTIFUNGAL SOLUTION MAXIMUM STRENGTH (TOLNAFTATE) LIQUID [RITE AID CORPORATION] | 3 | Current NDC, 2 package rows | 20241213_13a49826-f368-95f8-e063-6394a90adc4b.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 |
|---|
| 11822-9600-1 | 11822960001 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (11822-9600-1) / 30 mL in 1 BOTTLE, WITH APPLICATOR | 2024-03-14 | 2026-09-30 | No | No | Historical |