Hand sanitizer
- Product NDC
- 74881-009
- 11-digit product format
- 748810009
- Labeler code
- 74881
- Product ID
- 74881-009_b6bca74a-abf7-32a0-e053-2a95a90aacec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FLTR
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Huizhou Baozi Biotechnology Co.,Ltd.
- 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 |
|---|
| 74881-009-01 | Hand sanitizer | 50 mL in 1 BOTTLE | GEL | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 74881-009 | HAND SANITIZER (FLTR) GEL [HUIZHOU BAOZI BIOTECHNOLOGY CO.,LTD.] | 2 | Legacy NDC, 1 package rows | 20201219_b6a45750-4513-4836-e053-2a95a90a1a64.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 |
|---|
| 74881-009-01 | 74881000901 | 50 mL in 1 BOTTLE (74881-009-01) | 50 ml | 2020-07-27 | 0000-00-00 | No | No | Current |