BANITORE Alcohol Hand Rub
- Product NDC
- 56084-031
- 11-digit product format
- 560840031
- Labeler code
- 56084
- Product ID
- 56084-031_d9c807a5-c21a-e044-e053-2995a90a4770
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zhejiang RIFESHOW Cosmetics Co., Ltd.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-03-05
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 56084-031-01 | BANITORE Alcohol Hand Rub | 500 mL in 1 BOTTLE | LIQUID | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56084-031 | BANITORE ALCOHOL HAND RUB (ALCOHOL) LIQUID [ZHEJIANG RIFESHOW COSMETICS CO., LTD.] | 3 | Legacy NDC, 1 package rows | 20220310_d978d0af-8a86-0e97-e053-2a95a90a63e7.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 |
|---|
| 56084-031-01 | 56084003101 | 500 mL in 1 BOTTLE (56084-031-01) | 500 ml | 2022-03-05 | 0000-00-00 | No | No | Current |