tazza hand sanitizing foam
- Product NDC
- 76370-0022
- 11-digit product format
- 763700022
- Labeler code
- 76370
- Product ID
- 76370-0022_0fc6e0d5-ff65-fb0e-e063-6394a90a4043
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Tazza Brands East Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-17
- Substance
- ALCOHOL
- Active strength
- 63 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
- tazza hand sanitizing foam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 63 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 2396261 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76370-0022-1 | tazza hand sanitizing foam | 3785 mL in 1 BOTTLE | LIQUID | 3785 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76370-0022 | TAZZA HAND SANITIZING FOAM (ALCOHOL) LIQUID [TAZZA BRANDS EAST INC.] | 1 | Current NDC, 1 package rows | 20240208_0fc6e0d5-ff64-fb0e-e063-6394a90a4043.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 76370-0022-1 | 76370002201 | 3785 mL in 1 BOTTLE (76370-0022-1) | 3785 ml | 2024-01-17 | No | No | Historical |