Omax Cryofreeze Roll-On
- Product NDC
- 73036-001
- 11-digit product format
- 730360001
- Labeler code
- 73036
- Product ID
- 73036-001_a8a8718f-b41f-49c3-9633-a1b9cb2029d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Omax Health, Inc
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-08
- Marketing end
- 2022-05-15
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 85 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73036-001-01 | 73036000101 | 89 mL in 1 BOTTLE, WITH APPLICATOR (73036-001-01) | 89 ml | 2019-04-08 | 2022-05-15 | No | No | Current |