SAN X E2
- Product NDC
- 69884-706
- 11-digit product format
- 698840706
- Labeler code
- 69884
- Product ID
- 69884-706_2965dbef-0591-4303-e063-6394a90aeddc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Amerisan, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-31
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .12 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SAN X E2
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .12 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1053188 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69884-706-06 | SAN X E2 | 1250 mL in 1 BOTTLE | LIQUID | 1250 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69884-706 | SAN X E2 (BENZALKONIUM CHLORIDE) LIQUID [AMERISAN, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241218_d6e2f275-4609-24e6-e053-2995a90a8dd3.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 |
|---|
| 69884-706-06 | 69884070606 | 1250 mL in 1 BOTTLE (69884-706-06) | 1250 ml | 2022-01-31 | 0000-00-00 | No | No | Current |