Moxie Hand Sanitizing Gel
- Product NDC
- 77720-033
- 11-digit product format
- 777200033
- Labeler code
- 77720
- Product ID
- 77720-033_2f69f248-b382-6811-e063-6394a90aa8a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Skaffles Group
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-05-15
- Substance
- ALCOHOL
- Active strength
- 71 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
- Moxie Hand Sanitizing Gel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 71 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 2282911 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 77720-033-01 | Moxie Hand Sanitizing Gel | 500 mL in 1 PACKAGE | GEL | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 77720-033 | MOXIE HAND SANITIZING GEL (ALCOHOL) GEL [SKAFFLES GROUP] | 3 | Current NDC, 1 package rows | 20250304_fbb5cd9c-c9dc-42ed-9035-f57455ce092a.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 |
|---|
| 77720-033-01 | 77720003301 | 500 mL in 1 PACKAGE (77720-033-01) | 500 ml | 2024-05-15 | No | No | Current |