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Hibiclens
Hibiclens - 0234-0575-32 - (Chlorhexidine gluconate)
Drug Information of Hibiclens
| Product NDC: | 0234-0575 |
| Proprietary Name: | Hibiclens |
| Non Proprietary Name: | Chlorhexidine gluconate |
| Active Ingredient(s): | 213 g/1000mL & nbsp; Chlorhexidine gluconate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hibiclens
| Product NDC: | 0234-0575 |
| Labeler Name: | Molnlycke Health Care US, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA017768 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19760917 |
Package Information of Hibiclens
| Package NDC: | 0234-0575-32 |
| Package Description: | 946 mL in 1 BOTTLE (0234-0575-32) |
NDC Information of Hibiclens
| NDC Code | 0234-0575-32 |
| Proprietary Name | Hibiclens |
| Package Description | 946 mL in 1 BOTTLE (0234-0575-32) |
| Product NDC | 0234-0575 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorhexidine gluconate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19760917 |
| Marketing Category Name | NDA |
| Labeler Name | Molnlycke Health Care US, LLC |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 213 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
