Alcohol Free Hand Sanitizer
- Product NDC
- 60933-200
- 11-digit product format
- 609330200
- Labeler code
- 60933
- Product ID
- 60933-200_08c07ef8-6cc8-bd48-e063-6294a90a51b9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- FULLER INDUSTRIES, INC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-09-01
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alcohol Free Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1038799 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60933-200-00 | Alcohol Free Hand Sanitizer | 1000 mL in 1 BAG | AEROSOL, FOAM | 1000 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60933-200 | ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [FULLER INDUSTRIES, INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231030_0ebf85c5-21ee-4d14-b88f-d8c078791aef.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 |
|---|
| 60933-200-00 | 60933020000 | 1000 mL in 1 BAG (60933-200-00) | 1000 ml | 2017-09-01 | 0000-00-00 | No | No | Current |