Cryofreeze Roll-On Extra Strength
- Product NDC
- 73036-004
- 11-digit product format
- 730360004
- Labeler code
- 73036
- Product ID
- 73036-004_64a930f4-cdcb-4f10-bcce-8165ff87acdc
- 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
- 2022-03-16
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 85 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73036-004-01 | Cryofreeze Roll-On Extra Strength | 89 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 89 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73036-004 | CRYOFREEZE ROLL-ON EXTRA STRENGTH (MENTHOL, UNSPECIFIED FORM) GEL [OMAX HEALTH, INC] | 1 | Legacy NDC, 1 package rows | 20220322_61fbc467-c64f-4635-8abb-5dbd5a969179.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73036-004-01 | 73036000401 | 89 mL in 1 BOTTLE, WITH APPLICATOR (73036-004-01) | 89 ml | 2022-03-16 | 0000-00-00 | No | No | Current |