Wave Hand Sanitizer
- Product NDC
- 78754-001
- 11-digit product format
- 787540001
- Labeler code
- 78754
- Product ID
- 78754-001_a8fe89e5-023f-7b99-e053-2a95a90a2dc4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- C & A MARKETING, INC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-15
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 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 |
|---|
| 78754-001-08 | Wave Hand Sanitizer | 237 mL in 1 BOTTLE, PLASTIC | GEL | 237 | | 2 |
| 78754-001-16 | Wave Hand Sanitizer | 500 mL in 1 BOTTLE, PLASTIC | GEL | 500 | | 2 |
| 78754-001-28 | Wave Hand Sanitizer | 3790 mL in 1 BOTTLE, PLASTIC | GEL | 3790 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78754-001 | WAVE HAND SANITIZER (ALCOHOL) GEL [C & A MARKETING, INC.] | 2 | Legacy NDC, 3 package rows | 20200627_a84dfb7f-c453-4d01-e053-2995a90af0e6.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 |
|---|
| 78754-001-08 | 78754000108 | 237 mL in 1 BOTTLE, PLASTIC (78754-001-08) | 237 ml | 2020-06-15 | 0000-00-00 | No | No | Current |
| 78754-001-16 | 78754000116 | 500 mL in 1 BOTTLE, PLASTIC (78754-001-16) | 500 ml | 2020-06-15 | 0000-00-00 | No | No | Current |
| 78754-001-28 | 78754000128 | 3790 mL in 1 BOTTLE, PLASTIC (78754-001-28) | 3790 ml | 2020-06-15 | 0000-00-00 | No | No | Current |