ELLE ANTIBACTERIAL HAND WASH
- Product NDC
- 79165-112
- 11-digit product format
- 791650112
- Labeler code
- 79165
- Product ID
- 79165-112_a0fb57c0-f2b8-438c-b671-73de81dcbb8c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Alta Sales Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-03
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79165-112-01 | ELLE ANTIBACTERIAL HAND WASH | 500 mL in 1 BOTTLE | LIQUID | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79165-112 | ELLE ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [ALTA SALES INC] | 1 | Legacy NDC, 1 package rows | 20200908_b5faef98-ebbc-44a1-b6fc-b523e7aeb514.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 |
|---|
| 79165-112-01 | 79165011201 | 500 mL in 1 BOTTLE (79165-112-01) | 500 ml | 2020-09-03 | 0000-00-00 | No | No | Current |