HAND SANITIZER
- Product NDC
- 75613-007
- 11-digit product format
- 756130007
- Labeler code
- 75613
- Product ID
- 75613-007_939a9f8d-7942-4c11-bf1e-352d229d8032
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ningbo Lanzi Cosmetic Technology Co., Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-23
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 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 |
|---|
| 75613-007-01 | HAND SANITIZER | 8 mL in 1 BOTTLE, SPRAY | LIQUID | 8 | | 1 |
| 75613-007-02 | HAND SANITIZER | 10 mL in 1 BOTTLE, SPRAY | LIQUID | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75613-007 | HAND SANITIZER (ALCOHOL) LIQUID [NINGBO LANZI COSMETIC TECHNOLOGY CO., LTD] | 1 | Legacy NDC, 2 package rows | 20200623_ff1533e2-504d-43f9-85b7-b4afece87f91.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 |
|---|
| 75613-007-01 | 75613000701 | 8 mL in 1 BOTTLE, SPRAY (75613-007-01) | 8 ml | 2020-06-23 | 0000-00-00 | No | No | Current |
| 75613-007-02 | 75613000702 | 10 mL in 1 BOTTLE, SPRAY (75613-007-02) | 10 ml | 2020-06-23 | 0000-00-00 | No | No | Current |