chloraprep
Generic: chloraprep
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
chloraprep
Generic Name
chloraprep
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
SOLUTION
Routes
Active Ingredients
chlorhexidine gluconate 20 mg/mL, isopropyl alcohol .7 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1675
Product ID
51662-1675_44fe08e0-4e9d-8bd6-e063-6394a90a0e2b
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA021555
Listing Expiration
2026-12-31
Marketing Start
2024-05-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621675
Hyphenated Format
51662-1675
Supplemental Identifiers
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
chloraprep (source: ndc)
Generic Name
chloraprep (source: ndc)
Application Number
NDA021555 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
- .7 mL/mL
Packaging
- 1 APPLICATOR in 1 POUCH (51662-1675-1) / 1.75 mL in 1 APPLICATOR
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "44fe08e0-4e9d-8bd6-e063-6394a90a0e2b", "openfda": {"unii": ["MOR84MUD8E", "ND2M416302"], "spl_set_id": ["44fe08e0-4e9c-8bd6-e063-6394a90a0e2b"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 POUCH (51662-1675-1) / 1.75 mL in 1 APPLICATOR", "package_ndc": "51662-1675-1", "marketing_start_date": "20240513"}], "brand_name": "CHLORAPREP", "product_id": "51662-1675_44fe08e0-4e9d-8bd6-e063-6394a90a0e2b", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Cell Wall Integrity [PE]"], "product_ndc": "51662-1675", "generic_name": "CHLORAPREP", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CHLORAPREP", "active_ingredients": [{"name": "CHLORHEXIDINE GLUCONATE", "strength": "20 mg/mL"}, {"name": "ISOPROPYL ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "NDA021555", "marketing_category": "NDA", "marketing_start_date": "20240513", "listing_expiration_date": "20261231"}