dukal alcohol prep pad
Generic: isopropyl alcohol
Labeler: dukal llcDrug Facts
Product Profile
Brand Name
dukal alcohol prep pad
Generic Name
isopropyl alcohol
Labeler
dukal llc
Dosage Form
SWAB
Routes
Active Ingredients
isopropyl alcohol .7 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65517-0001
Product ID
65517-0001_43f80758-c08e-b56e-e063-6294a90a8ad5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2010-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
655170001
Hyphenated Format
65517-0001
Supplemental Identifiers
RxCUI
UNII
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
dukal alcohol prep pad (source: ndc)
Generic Name
isopropyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 mL/mL
Packaging
- .4 mL in 1 POUCH (65517-0001-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43f80758-c08e-b56e-e063-6294a90a8ad5", "openfda": {"unii": ["ND2M416302"], "rxcui": ["797544"], "spl_set_id": ["953b0dd6-a667-4146-815e-6845aba0309b"], "manufacturer_name": ["Dukal LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".4 mL in 1 POUCH (65517-0001-1)", "package_ndc": "65517-0001-1", "marketing_start_date": "20100501"}], "brand_name": "Dukal Alcohol Prep Pad", "product_id": "65517-0001_43f80758-c08e-b56e-e063-6294a90a8ad5", "dosage_form": "SWAB", "product_ndc": "65517-0001", "generic_name": "ISOPROPYL ALCOHOL", "labeler_name": "Dukal LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dukal Alcohol Prep Pad", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100501", "listing_expiration_date": "20261231"}