progel max hand sanitizer
Generic: alcohol
Labeler: delta pharma inc.Drug Facts
Product Profile
Brand Name
progel max hand sanitizer
Generic Name
alcohol
Labeler
delta pharma inc.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 80 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
66353-117
Product ID
66353-117_249e095b-fba3-b6a2-e063-6394a90a7459
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-06-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66353117
Hyphenated Format
66353-117
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
progel max hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mL/100mL
Packaging
- 350 mL in 1 BOTTLE (66353-117-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "249e095b-fba3-b6a2-e063-6394a90a7459", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1039339"], "spl_set_id": ["a607897c-c398-1931-e053-2a95a90ae483"], "manufacturer_name": ["Delta Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "350 mL in 1 BOTTLE (66353-117-01)", "package_ndc": "66353-117-01", "marketing_start_date": "20200612"}], "brand_name": "ProGel Max Hand Sanitizer", "product_id": "66353-117_249e095b-fba3-b6a2-e063-6394a90a7459", "dosage_form": "LIQUID", "product_ndc": "66353-117", "generic_name": "ALCOHOL", "labeler_name": "Delta Pharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ProGel Max Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "80 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200612", "listing_expiration_date": "20261231"}