Hands-free Surgical Gel
- Product NDC
- 40796-003
- 11-digit product format
- 407960003
- Labeler code
- 40796
- Product ID
- 40796-003_a5838ccf-1046-e7df-e053-2995a90a9663
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hands-free Surgical Gel
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- Jiangxi Baiyi Weishi Medical Technology Co., Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-13
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL; PROPYL ALCOHOL
- Active strength
- 325 mL/500mL; g/500mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 40796-003-01 | Hands-free Surgical Gel | 500 mL in 1 BOTTLE | GEL | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 40796-003 | HANDS-FREE SURGICAL GEL GEL [JIANGXI BAIYI WEISHI MEDICAL TECHNOLOGY CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200514_a5838ccf-1045-e7df-e053-2995a90a9663.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 40796-003-01 | 40796000301 | 500 mL in 1 BOTTLE | 500 ml | Historical |