Zilactin
- Product NDC
- 72751-0301
- 11-digit product format
- 727510301
- Labeler code
- 72751
- Product ID
- 72751-0301_d21c275e-697d-e95e-e053-2a95a90ad633
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzyl alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Applied Laboratories, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2005-06-30
- Marketing end
- 0000-00-00
- Substance
- BENZYL ALCOHOL
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72751-0301-1 | 72751030101 | 1 TUBE in 1 CARTON (72751-0301-1) > 7.1 g in 1 TUBE | 1 tube | 2005-06-30 | 0000-00-00 | No | No | Current |