alcohol prep pad
Generic: alcohol prep pad
Labeler: aso llcDrug Facts
Product Profile
Brand Name
alcohol prep pad
Generic Name
alcohol prep pad
Labeler
aso llc
Dosage Form
LIQUID
Routes
Active Ingredients
isopropyl alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
51142-444
Product ID
51142-444_25da293c-7ff5-8fe3-e063-6394a90a9af1
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2018-09-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51142444
Hyphenated Format
51142-444
Supplemental Identifiers
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
alcohol prep pad (source: ndc)
Generic Name
alcohol prep pad (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- .4 mL in 1 POUCH (51142-444-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "25da293c-7ff5-8fe3-e063-6394a90a9af1", "openfda": {"unii": ["ND2M416302"], "spl_set_id": ["7481bfb9-2baf-b1ec-e053-2991aa0ad2de"], "manufacturer_name": ["ASO LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".4 mL in 1 POUCH (51142-444-01)", "package_ndc": "51142-444-01", "marketing_start_date": "20180924"}], "brand_name": "Alcohol Prep Pad", "product_id": "51142-444_25da293c-7ff5-8fe3-e063-6394a90a9af1", "dosage_form": "LIQUID", "product_ndc": "51142-444", "generic_name": "Alcohol Prep Pad", "labeler_name": "ASO LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol Prep Pad", "active_ingredients": [{"name": "ISOPROPYL ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}