Hand Wash
- Product NDC
- 41250-661
- 11-digit product format
- 412500661
- Labeler code
- 41250
- Product ID
- 41250-661_4b33dcaa-f3c2-467e-e063-6294a90a4e16
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Meijer, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-12-20
- 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 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-661-45 | Hand Wash | 946 mL in 1 BOTTLE, PLASTIC | LIQUID | 946 | | 14 |
| 41250-661-96 | Hand Wash | 221 mL in 1 BOTTLE, PUMP | LIQUID | 221 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-661 | HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [MEIJER DISTRIBUTION, INC] | 12 | Current NDC, Legacy NDC, 2 package rows | 20250311_8fbbc798-ac00-4755-a2c2-5cd5b5c01ae4.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 |
|---|
| 41250-661-45 | 41250066145 | 946 mL in 1 BOTTLE, PLASTIC (41250-661-45) | 946 ml | 2019-12-20 | 0000-00-00 | No | No | Current |
| 41250-661-96 | 41250066196 | 221 mL in 1 BOTTLE, PUMP (41250-661-96) | 221 ml | 2019-12-20 | 0000-00-00 | No | No | Current |