BZK
- Product NDC
- 0404-6735
- 11-digit product format
- 004046735
- Labeler code
- 0404
- Product ID
- 0404-6735_1522e337-1394-24fa-e063-6394a90ae000
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Henry Schein Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-01-07
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .0013 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BZK
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .0013 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0404-6735-01 | BZK | 2.5 g in 1 PACKET | LIQUID | 2.5 | | 5 |
| 0404-6735-01 | BZK | 100 in 1 BOX | LIQUID | 100 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0404-6735 | BZK (BENZALKONIUM CHLORIDE) LIQUID [HENRY SCHEIN INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240404_ff877b63-fa58-4770-a882-694eda33203b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0404-6735-01 | 00404673501 | 100 PACKET in 1 BOX (0404-6735-01) / 2.5 g in 1 PACKET | 100 packet | 2016-12-01 | No | No | Current |