Antiseptic
- Product NDC
- 47682-316
- 11-digit product format
- 476820316
- Labeler code
- 47682
- Product ID
- 47682-316_3e4ed1ac-fdd3-6cfb-e063-6294a90a58c0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Unifirst First Aid Corporation
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-05-16
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 g/L
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antiseptic
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 g/L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1039012 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 47682-316-02 | Antiseptic | 0.0591 L in 1 BOTTLE, SPRAY | LIQUID | 0.0591 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47682-316 | ANTISEPTIC (BENZALKONIUM CHLORIDE) LIQUID [UNIFIRST FIRST AID CORPORATION] | 8 | Current NDC, Legacy NDC, 1 package rows | 20240117_a0f58025-2c50-45dc-94db-cacbd4cf604c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47682-316-02 | 47682031602 | .0591 L in 1 BOTTLE, SPRAY (47682-316-02) | 2016-05-16 | 0000-00-00 | No | No | Current |