Hand Wash
- Product NDC
- 69790-466
- 11-digit product format
- 697900466
- Labeler code
- 69790
- Product ID
- 69790-466_4b099bfa-cd9d-d843-e063-6294a90accae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- ULINE
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-02-17
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 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
- Hand Wash
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 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 |
|---|
| 69790-466-96 | Hand Wash | 221 mL in 1 BOTTLE, PLASTIC | SOAP | 221 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69790-466 | HAND WASH (BENZALKONIUM CHLORIDE) SOAP [ULINE] | 10 | Current NDC, Legacy NDC, 1 package rows | 20240929_5a4d6fb7-486a-448c-b379-726adf60e411.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 |
|---|
| 69790-466-96 | 69790046696 | 221 mL in 1 BOTTLE, PLASTIC (69790-466-96) | 221 ml | 2016-02-17 | 0000-00-00 | No | No | Current |