Chlorhexidine Gluconate
- Product NDC
- 70518-4494
- 11-digit product format
- 705184494
- Labeler code
- 70518
- Product ID
- 70518-4494_40a7bbe1-0774-2617-e063-6294a90a6aa7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorhexidine Gluconate
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077789
- Marketing category
- ANDA
- Marketing start
- 2025-10-08
- Substance
- CHLORHEXIDINE GLUCONATE
- Active strength
- 1.2 mg/mL
- Pharmacologic classes
- Decreased Cell Wall Integrity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MOR84MUD8E | CHLORHEXIDINE GLUCONATE | 18472-51-0 | CHLORHEXIDINE GLUCONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4494-0 | 70518449400 | 473 mL in 1 BOTTLE (70518-4494-0) | 473 ml | 2025-10-08 | No | No | Historical |