Fuzion AB Foam
- Product NDC
- 66949-111
- 11-digit product format
- 669490111
- Labeler code
- 66949
- Product ID
- 66949-111_46de4539-36b3-af75-e063-6294a90acfff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zep Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-03-10
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 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
- Fuzion AB Foam
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .13 g/100mL |
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 |
|---|
| 66949-111-16 | Fuzion AB Foam | 4800 mL in 1 CASE | LIQUID | 4800 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66949-111 | FUZION AB FOAM (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241120_b43ea64e-f7db-2250-e053-2995a90a43b3.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 |
|---|
| 66949-111-16 | 66949011116 | 4800 mL in 1 CASE (66949-111-16) | 4800 ml | 2017-03-10 | 0000-00-00 | No | No | Current |