Wave Hand Sanitizer
- Product NDC
- 77566-831
- 11-digit product format
- 775660831
- Labeler code
- 77566
- Product ID
- 77566-831_ab9d1cfc-efb8-624d-e053-2995a90a67af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Earthlite, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-29
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 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 |
|---|
| 77566-831-81 | Wave Hand Sanitizer | 287 mL in 1 BOTTLE, SPRAY | LIQUID | 287 | | 2 |
| 77566-831-11 | Wave Hand Sanitizer | 3780 mL in 1 BOTTLE, PLASTIC | LIQUID | 3780 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 77566-831 | WAVE HAND SANITIZER (ALCOHOL) LIQUID [EARTHLITE, LLC] | 2 | Legacy NDC, 1 package rows | 20200731_ab9d484a-c0cb-0199-e053-2995a90a37c1.zip |
| 77566-831 | WAVE HAND SANITIZER (ALCOHOL) LIQUID [EARTHLITE, LLC] | 1 | Legacy NDC, 1 package rows | 20200731_ab9d796b-1b7f-690d-e053-2995a90a6749.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 |
|---|
| 77566-831-11 | 77566083111 | 3780 mL in 1 BOTTLE, PLASTIC (77566-831-11) | 3780 ml | 2020-07-29 | 0000-00-00 | No | No | Current |
| 77566-831-81 | 77566083181 | 287 mL in 1 BOTTLE, SPRAY (77566-831-81) | 287 ml | 2020-07-29 | 0000-00-00 | No | No | Current |