ZILXI
- Product NDC
- 72356-103
- 11-digit product format
- 723560103
- Labeler code
- 72356
- Product ID
- 72356-103_4a338f8a-b749-4d69-b8aa-1b1b5ebb77b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Journey Medical Corporation
- Application
- NDA213690
- Marketing category
- NDA
- Marketing start
- 2020-10-01
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 15 mg/g
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72356-103 | ZILXI (MINOCYCLINE) AEROSOL, FOAM [JOURNEY MEDICAL CORPORATION] | 6 | Legacy NDC | 20220916_116f9ade-1bdc-4162-98d8-d3a0c592f419.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72356-103-03 | 72356010303 | 1 CAN in 1 CARTON (72356-103-03) > 30 g in 1 CAN | 1 can | 2020-10-01 | 0000-00-00 | No | No | Current |
| 72356-103-90 | 72356010390 | 1 CAN in 1 CARTON (72356-103-90) > 7 g in 1 CAN | 1 can | 2020-10-01 | 0000-00-00 | No | No | Current |