BT21 HAND SANITIZER
- Product NDC
- 78967-020
- 11-digit product format
- 789670020
- Labeler code
- 78967
- Product ID
- 78967-020_6ed2b8ca-d68a-4af7-b2cf-9bc3d6fc39ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- BALLON BLANC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 42 mL/60mL
- 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 |
|---|
| 78967-020-01 | BT21 HAND SANITIZER | 60 mL in 1 BOTTLE | GEL | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78967-020 | BT21 HAND SANITIZER (ALCOHOL) GEL [BALLON BLANC] | 1 | Legacy NDC, 1 package rows | 20200922_c105e108-c9a1-4a1d-bdbd-51101a7dd7a8.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 |
|---|
| 78967-020-01 | 78967002001 | 60 mL in 1 BOTTLE (78967-020-01) | 60 ml | 2020-09-01 | 0000-00-00 | No | No | Current |