SUEZ Gel Formula
- Product NDC
- 80896-010
- 11-digit product format
- 808960010
- Labeler code
- 80896
- Product ID
- 80896-010_b25beeda-aca2-b598-e053-2a95a90a5716
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SUEZ Gel Formula
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SUEZ Water Technologies & Solutions
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-23
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- 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 |
|---|
| 80896-010-12 | SUEZ Gel Formula | 1040875 mL in 1 BOTTLE | GEL | 1040875 | | 1 |
| 80896-010-17 | SUEZ Gel Formula | 3785 mL in 1 BOTTLE | GEL | 3785 | | 1 |
| 80896-010-18 | SUEZ Gel Formula | 355 mL in 1 BOTTLE | GEL | 355 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80896-010 | SUEZ GEL FORMULA GEL [SUEZ WATER TECHNOLOGIES & SOLUTIONS] | 1 | Legacy NDC, 3 package rows | 20201027_b25bf001-a9d1-3630-e053-2a95a90af9fd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80896-010-12 | 80896001012 | 1040875 mL in 1 BOTTLE (80896-010-12) | 1040875 ml | 2020-10-23 | 0000-00-00 | No | No | Current |
| 80896-010-17 | 80896001017 | 3785 mL in 1 BOTTLE (80896-010-17) | 3785 ml | 2020-10-23 | 0000-00-00 | No | No | Current |
| 80896-010-18 | 80896001018 | 355 mL in 1 BOTTLE (80896-010-18) | 355 ml | 2020-10-23 | 0000-00-00 | No | No | Current |