Chlorhexidine Gluconate
- Product NDC
- 21695-025
- 11-digit product format
- 216950025
- Labeler code
- 21695
- Product ID
- 21695-025_d42b0f1d-8930-4b69-9624-8d6c500caba8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorhexidine Gluconate
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077789
- Marketing category
- ANDA
- Marketing start
- 2009-08-01
- Marketing end
- 0000-00-00
- Substance
- CHLORHEXIDINE GLUCONATE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Decreased Cell Wall Integrity [PE]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-025-16 | Chlorhexidine Gluconate | 473 mL in 1 BOTTLE | RINSE | 473 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-025 | CHLORHEXIDINE GLUCONATE RINSE [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20101126_d42b0f1d-8930-4b69-9624-8d6c500caba8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 21695-025-16 | 21695002516 | 473 mL in 1 BOTTLE | 473 ml | Historical |