Benzethonium Chloride Solution
- Product NDC
- 54340-249
- 11-digit product format
- 543400249
- Labeler code
- 54340
- Product ID
- 54340-249_0a70d7e2-d2a0-27cc-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dial Complete Spring Water Foaming Antibacterial Hand Wash
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- The Dial Corporation, A Henkel Company
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-01-05
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54340-249-01 | Benzethonium Chloride Solution | 221 mL in 1 BOTTLE, PUMP | SOLUTION | 221 | | 1 |
| 54340-249-02 | Benzethonium Chloride Solution | 946 mL in 1 BOTTLE, DISPENSING | SOLUTION | 946 | | 1 |
| 54340-249-03 | Benzethonium Chloride Solution | 1180 mL in 1 BOTTLE, DISPENSING | SOLUTION | 1180 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54340-249 | BENZETHONIUM CHLORIDE SOLUTION (DIAL COMPLETE SPRING WATER FOAMING ANTIBACTERIAL HAND WASH) SOLUTION [THE DIAL CORPORATION, A HENKEL COMPANY] | 1 | Legacy NDC, 3 package rows | 20150312_0a70d7e2-d29f-27cc-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54340-249-01 | 54340024901 | 221 mL in 1 BOTTLE, PUMP | 221 ml | Historical |
| 54340-249-02 | 54340024902 | 946 mL in 1 BOTTLE, DISPENSING | 946 ml | Historical |
| 54340-249-03 | 54340024903 | 1180 mL in 1 BOTTLE, DISPENSING | 1180 ml | Historical |