LactiGo
- Product NDC
- 72481-102
- 11-digit product format
- 724810102
- Labeler code
- 72481
- Product ID
- 72481-102_4dda6ac4-d84a-69a6-e063-6394a90a3c54
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- LactiGo, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-25
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 15 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LactiGo
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 15 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 2739292 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72481-102-32 | LactiGo | 946 mL in 1 BOTTLE, PUMP | GEL | 946 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72481-102-32 | 72481010232 | 946 mL in 1 BOTTLE, PUMP (72481-102-32) | 946 ml | 2026-03-25 | No | No | Historical |