Antibacterial Hand Wash
- Product NDC
- 69790-488
- 11-digit product format
- 697900488
- Labeler code
- 69790
- Product ID
- 69790-488_4b09a24b-e82c-d0ea-e063-6294a90a5ea9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride 0.13%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Uline
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-05-27
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.313 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antibacterial Hand Wash
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.313 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1046593 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69790-488-08 | Antibacterial Hand Wash | 3785 mL in 1 BOTTLE, PLASTIC | LIQUID | 3785 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69790-488 | ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE 0.13%) LIQUID [ULINE] | 9 | Current NDC, Legacy NDC, 1 package rows | 20240929_9e7a97a0-f3dd-40cf-b25e-8ebb65693926.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 |
|---|
| 69790-488-08 | 69790048808 | 3785 mL in 1 BOTTLE, PLASTIC (69790-488-08) | 3785 ml | 2018-05-27 | 0000-00-00 | No | No | Current |