Sanix Alcohol Hand Rub
- Product NDC
- 51326-900
- 11-digit product format
- 513260900
- Labeler code
- 51326
- Product ID
- 51326-900_2af17da6-253d-4958-92ce-2dc70987b669
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Topiderm, Inc
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-17
- Substance
- ALCOHOL
- Active strength
- .62 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sanix Alcohol Hand Rub
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | .62 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581660 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51326-900-08 | Sanix Alcohol Hand Rub | 240 mL in 1 BOTTLE | LIQUID | 240 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51326-900 | SANIX ALCOHOL HAND RUB (ALCOHOL) LIQUID [TOPIDERM, INC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231201_a4fbb714-4f20-400a-ab98-f1c8807ce6fc.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 |
|---|
| 51326-900-08 | 51326090008 | 240 mL in 1 BOTTLE (51326-900-08) | 240 ml | 2020-03-17 | 0000-00-00 | No | No | Current |