AKOLKOL TOENAIL FUNGUS TREATMENT
- Product NDC
- 84989-021
- 11-digit product format
- 849890021
- Labeler code
- 84989
- Product ID
- 84989-021_5121c341-e5ea-2b36-e063-6394a90a93b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GLYCERIN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shantou Ximonth Biotechnology Co., Ltd.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-06
- Substance
- ALOE BARBADENSIS LEAF; CENTELLA ASIATICA LEAF
- Active strength
- .003; .003 mg/30mg; mg/30mg
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AKOLKOL TOENAIL FUNGUS TREATMENT
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALOE BARBADENSIS LEAF | .003 mg/30mg |
| CENTELLA ASIATICA LEAF | .003 mg/30mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZY81Z83H0X, 6810070TYD |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84989-021-01 | AKOLKOL TOENAIL FUNGUS TREATMENT | 30 mg in 1 BOTTLE, PLASTIC | LIQUID | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84989-021-01 | 84989002101 | 30 mg in 1 BOTTLE, PLASTIC (84989-021-01) | 30 mg | 2026-05-06 | No | No | Historical |