SeaLuxe Hand Sanitizer
- Product NDC
- 79959-001
- 11-digit product format
- 799590001
- Labeler code
- 79959
- Product ID
- 79959-001_ae2d7bff-6daf-61e0-e053-2a95a90a3216
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- APR Beauty Group Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-28
- 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 |
|---|
| 79959-001-24 | SeaLuxe Hand Sanitizer | 240 mL in 1 BOTTLE | GEL | 240 | | 3 |
| 79959-001-35 | SeaLuxe Hand Sanitizer | 315 mL in 1 BOTTLE | GEL | 315 | | 3 |
| 79959-001-50 | SeaLuxe Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79959-001 | SEALUXE HAND SANITIZER (ETHYL ALCOHOL) GEL [APR BEAUTY GROUP INC.] | 3 | Legacy NDC, 3 package rows | 20200909_ac7d5dcb-54bf-43ba-a56b-52969c89ccac.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 |
|---|
| 79959-001-24 | 79959000124 | 240 mL in 1 BOTTLE (79959-001-24) | 240 ml | 2020-08-28 | 0000-00-00 | No | No | Current |
| 79959-001-35 | 79959000135 | 315 mL in 1 BOTTLE (79959-001-35) | 315 ml | 2020-08-28 | 0000-00-00 | No | No | Current |
| 79959-001-50 | 79959000150 | 500 mL in 1 BOTTLE (79959-001-50) | 500 ml | 2020-08-28 | 0000-00-00 | No | No | Current |