warnings
For external use only
Hibiclens
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Hibiclens
- Generic name
- CHLORHEXIDINE GLUCONATE
- Manufacturer
- Molnlycke Health Care
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4275eb53-1a7e-4a91-aac1-1085f40fac88
- SPL ID
- 29f3a722-b70e-15f6-e063-6294a90a474f
- Version
- 13
- Effective date
- 2024-12-23
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:36:51
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 017768 | derived:openfda.application_number |
| application number | NDA017768 | openfda.application_number | |
| brand name | Hibiclens | openfda.brand_name | |
| generic name | CHLORHEXIDINE GLUCONATE | openfda.generic_name | |
| manufacturer name | Molnlycke Health Care | openfda.manufacturer_name | |
| ndc | package | 0234-0575-91 | openfda.package_ndc |
| ndc | package | 0234-0575-32 | openfda.package_ndc |
| ndc | package | 0234-0575-16 | openfda.package_ndc |
| ndc | package | 0234-0575-08 | openfda.package_ndc |
| ndc | package | 0234-0575-04 | openfda.package_ndc |
| ndc | product | 0234-0575 | openfda.product_ndc |
| ndc11 | package | 00234057532 | derived:openfda.package_ndc |
| ndc11 | package | 00234057504 | derived:openfda.package_ndc |
| ndc11 | package | 00234057516 | derived:openfda.package_ndc |
| ndc11 | package | 00234057591 | derived:openfda.package_ndc |
| ndc11 | package | 00234057508 | derived:openfda.package_ndc |
| rxcui | 834167 | openfda.rxcui | |
| rxcui | 211365 | openfda.rxcui | |
| spl id | 29f3a722-b70e-15f6-e063-6294a90a474f | id | |
| spl set id | 4275eb53-1a7e-4a91-aac1-1085f40fac88 | set_id | |
| unii | MOR84MUD8E | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Allergy alert: This product may cause a severe allergic reaction. Symptoms may include: wheezing/difficulty breathing shock facial swelling hives rash If an allergic reaction occurs, stop use and seek medical help right away.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.