Foaming Hand Sanitizer
- Product NDC
- 50021-020
- 11-digit product format
- 500210020
- Labeler code
- 50021
- Product ID
- 50021-020_20af4f6c-4c3d-c789-e063-6294a90a0307
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Empack Spraytech Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-11-11
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Foaming Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 616805 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50021-020-01 | Foaming Hand Sanitizer | 550 mL in 1 BOTTLE, PUMP | SOLUTION | 550 | | 2 |
| 50021-020-02 | Foaming Hand Sanitizer | 3785 mL in 1 BOTTLE, PUMP | SOLUTION | 3785 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50021-020 | FOAMING HAND SANITIZER (ALCOHOL) SOLUTION [EMPACK SPRAYTECH INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241215_8bb072f2-9cd4-499d-9d7f-7166451b8f20.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 |
|---|
| 50021-020-01 | 50021002001 | 550 mL in 1 BOTTLE, PUMP (50021-020-01) | 550 ml | 2020-11-11 | 0000-00-00 | No | No | Current |
| 50021-020-02 | 50021002002 | 3785 mL in 1 BOTTLE, PUMP (50021-020-02) | 3785 ml | 2020-11-11 | 0000-00-00 | No | No | Current |