LactiGo
- Product NDC
- 72481-101
- 11-digit product format
- 724810101
- Labeler code
- 72481
- Product ID
- 72481-101_213e8489-762b-461f-e063-6394a90a64a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- LactiGo, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-21
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 12.5 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
- LactiGo
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 12.5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 866128 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72481-101-03 | LactiGo | 100 mL in 1 BOTTLE, PUMP | GEL | 100 | | 4 |
| 72481-101-32 | LactiGo | 946 mL in 1 BOTTLE, PUMP | GEL | 946 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72481-101 | LACTIGO (MENTHOL) GEL [LACTIGO, INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240905_849c3601-2bc8-0991-e053-2a91aa0a5e7f.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 |
|---|
| 72481-101-03 | 72481010103 | 100 mL in 1 BOTTLE, PUMP (72481-101-03) | 100 ml | 2019-03-21 | 0000-00-00 | No | No | Current |
| 72481-101-32 | 72481010132 | 946 mL in 1 BOTTLE, PUMP (72481-101-32) | 946 ml | 2024-08-30 | | No | No | Current |