Antibacterial
- Product NDC
- 71020-003
- 11-digit product format
- 710200003
- Labeler code
- 71020
- Product ID
- 71020-003_513c9c2a-c06a-afb2-e063-6394a90a2f67
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Sante Manufcaturing Inc
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-10-08
- 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
- Antibacterial
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71020-003-32 | Antibacterial | 947 mL in 1 BOTTLE, PLASTIC | LIQUID | 947 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71020-003 | ANTIBACTERIAL (BENZALKONIUM CHLORIDE) LIQUID [SANTE MANUFCATURING INC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250109_3e5c5148-3196-2899-e054-00144ff8d46c.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 |
|---|
| 71020-003-32 | 71020000332 | 947 mL in 1 BOTTLE, PLASTIC (71020-003-32) | 947 ml | 2016-10-08 | 0000-00-00 | No | No | Current |