ALOE SCENTED HAND SANITIZER
- Product NDC
- 80684-120
- 11-digit product format
- 806840120
- Labeler code
- 80684
- Product ID
- 80684-120_2ef273fb-aeeb-bf0a-e063-6294a90a7ec9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- FOURSTAR GROUP USA, INC.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-08-15
- 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
- ALOE SCENTED 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 | 582753 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80684-120-00 | ALOE SCENTED HAND SANITIZER | 89 mL in 1 BOTTLE | LIQUID | 89 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80684-120 | ALOE SCENTED HAND SANITIZER (ALCOHOL) LIQUID [FOURSTAR GROUP USA, INC.] | 2 | Current NDC, 1 package rows | 20250227_aacde143-ecf1-47ce-ada3-8e74551d0659.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 |
|---|
| 80684-120-00 | 80684012000 | 89 mL in 1 BOTTLE (80684-120-00) | 89 ml | 2023-08-15 | No | No | Current |