dermacinrx clorhexacin
Generic: mupirocin ointment
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
dermacinrx clorhexacin
Generic Name
mupirocin ointment
Labeler
puretek corporation
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
59088-391
Product ID
59088-391_292fb349-6c9f-d1dd-e063-6394a90a5ed9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2016-06-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088391
Hyphenated Format
59088-391
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
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
dermacinrx clorhexacin (source: ndc)
Generic Name
mupirocin ointment (source: ndc)
Resolved Composition
Strengths
- 2 %
- 22 g
- 4 %
- 5.0 %
Packaging
- 1 KIT in 1 CARTON (59088-391-00) * 237 mL in 1 BOTTLE, PLASTIC (0116-1061-08) * 118 mL in 1 TUBE (59088-333-08) * 1 TUBE in 1 CARTON (45802-112-22) / 22 g in 1 TUBE
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "292fb349-6c9f-d1dd-e063-6394a90a5ed9", "openfda": {"rxcui": ["106346", "211365", "259090"], "spl_set_id": ["3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (59088-391-00) * 237 mL in 1 BOTTLE, PLASTIC (0116-1061-08) * 118 mL in 1 TUBE (59088-333-08) * 1 TUBE in 1 CARTON (45802-112-22) / 22 g in 1 TUBE", "package_ndc": "59088-391-00", "marketing_start_date": "20160602"}], "brand_name": "DermacinRx Clorhexacin", "product_id": "59088-391_292fb349-6c9f-d1dd-e063-6394a90a5ed9", "dosage_form": "KIT", "product_ndc": "59088-391", "generic_name": "Mupirocin Ointment", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DermacinRx Clorhexacin", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160602", "listing_expiration_date": "20261231"}