Blue Wave
- Product NDC
- 77356-835
- 11-digit product format
- 773560835
- Labeler code
- 77356
- Product ID
- 77356-835_a7492f91-174e-2ba5-e053-2995a90a8f47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Adonis, LLC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-01
- 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 |
|---|
| 77356-835-01 | Blue WaveHand Sanitizer | 236 mL in 1 BOTTLE | GEL | 236 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 77356-835 | BLUE WAVE HAND SANITIZER (ETHYL ALCOHOL) GEL [ADONIS, LLC.] | 1 | Legacy NDC, 1 package rows | 20200605_5f7b846f-57cc-4ea7-bf06-5f840c8d201d.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 |
|---|
| 77356-835-01 | 77356083501 | 236 mL in 1 BOTTLE (77356-835-01) | 236 ml | 2020-05-01 | 0000-00-00 | No | No | Current |