Hand sanitizer
- Product NDC
- 90081-008
- 11-digit product format
- 900810008
- Labeler code
- 90081
- Product ID
- 90081-008_b176506b-8191-390e-e053-2a95a90af130
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FLTR
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- FLTR, INC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-27
- 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 |
|---|
| 90081-008-01 | Hand sanitizer | 50 mL in 1 BOTTLE | GEL | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 90081-008 | HAND SANITIZER (FLTR) GEL [FLTR, INC.] | 1 | Legacy NDC, 1 package rows | 20201013_b176506b-8192-390e-e053-2a95a90af130.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 |
|---|
| 90081-008-01 | 90081000801 | 50 mL in 1 BOTTLE (90081-008-01) | 50 ml | 2020-07-27 | 0000-00-00 | No | No | Current |