Bee Well
- Product NDC
- 80655-420
- 11-digit product format
- 806550420
- Labeler code
- 80655
- Product ID
- 80655-420_a1857e6c-4ca1-4ee4-a1ad-3743fb0a5ff4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Isopropyl alcohol
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Bee Well LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-10
- Marketing end
- 0000-00-00
- Substance
- ISOPROPYL ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80655-420-69 | Bee WellHand Sanitizer | 59 mL in 1 BOTTLE | SPRAY | 59 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80655-420 | BEE WELL HAND SANITIZER (ISOPROPYL ALCOHOL) SPRAY [BEE WELL LLC] | 1 | Legacy NDC, 1 package rows | 20200926_05973008-b160-46a8-add6-1a4d5509cb33.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 |
|---|
| 80655-420-69 | 80655042069 | 59 mL in 1 BOTTLE (80655-420-69) | 59 ml | 2020-09-10 | 0000-00-00 | No | No | Current |