Benzalkonium Chloride
- Product NDC
- 79903-167
- 11-digit product format
- 799030167
- Labeler code
- 79903
- Product ID
- 79903-167_4bd556bf-02a2-1bce-e063-6294a90a7168
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Walmart Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-11-18
- 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
- Benzalkonium Chloride
- 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 |
|---|
| 79903-167-50 | Benzalkonium Chloride | 1470 mL in 1 BOTTLE, PLASTIC | GEL | 1470 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79903-167 | BENZALKONIUM CHLORIDE GEL [WAL-MART STORES, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241017_99fba457-0eea-4c0b-987f-6a1690f503fb.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 |
|---|
| 79903-167-50 | 79903016750 | 1470 mL in 1 BOTTLE, PLASTIC (79903-167-50) | 1470 ml | 2022-12-15 | 0000-00-00 | No | No | Current |