advanced alcohol gel sanitizer

Generic: alcohol

Labeler: betco corporation, ltd
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name advanced alcohol gel sanitizer
Generic Name alcohol
Labeler betco corporation, ltd
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol .7 mL/mL

Manufacturer
Betco Corporation, Ltd

Identifiers & Regulatory

Product NDC 65601-801
Product ID 65601-801_4b08e38b-43e8-1e6d-e063-6394a90a6422
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2019-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65601801
Hyphenated Format 65601-801

Supplemental Identifiers

RxCUI
581662
UPC
0700427027405 0700427028242 0700427027894 0700427029812 0700427031723 0700427027771
UNII
3K9958V90M

Packaging Origin

Original Packager
true

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 advanced alcohol gel sanitizer (source: ndc)
Generic Name alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .7 mL/mL
source: ndc
Packaging
  • 3780 mL in 1 BOTTLE, PLASTIC (65601-801-04)
  • 900 mL in 1 BAG (65601-801-19)
  • 1000 mL in 1 BAG (65601-801-29)
  • 208198 mL in 1 DRUM (65601-801-55)
  • 550 mL in 1 BOTTLE, PUMP (65601-801-57)
  • 1041000 mL in 1 CONTAINER (65601-801-99)
source: ndc

Packages (6)

65601-801-04 3780 mL in 1 BOTTLE, PLASTIC (65601-801-04) 65601-801-19 900 mL in 1 BAG (65601-801-19) 65601-801-29 1000 mL in 1 BAG (65601-801-29) 65601-801-55 208198 mL in 1 DRUM (65601-801-55) 65601-801-57 550 mL in 1 BOTTLE, PUMP (65601-801-57) 65601-801-99 1041000 mL in 1 CONTAINER (65601-801-99)

Ingredients (1)

alcohol (.7 mL/mL)

Linked Drug Pages (1)

Advanced Alcohol Gel Sanitizer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4b08e38b-43e8-1e6d-e063-6394a90a6422", "openfda": {"upc": ["0700427027405", "0700427028242", "0700427027894", "0700427029812", "0700427031723", "0700427027771"], "unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["a23b997c-b010-5985-e053-2995a90aadf3"], "manufacturer_name": ["Betco Corporation, Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3780 mL in 1 BOTTLE, PLASTIC (65601-801-04)", "package_ndc": "65601-801-04", "marketing_start_date": "20190801"}, {"sample": false, "description": "900 mL in 1 BAG (65601-801-19)", "package_ndc": "65601-801-19", "marketing_start_date": "20190801"}, {"sample": false, "description": "1000 mL in 1 BAG (65601-801-29)", "package_ndc": "65601-801-29", "marketing_start_date": "20190801"}, {"sample": false, "description": "208198 mL in 1 DRUM (65601-801-55)", "package_ndc": "65601-801-55", "marketing_start_date": "20190801"}, {"sample": false, "description": "550 mL in 1 BOTTLE, PUMP (65601-801-57)", "package_ndc": "65601-801-57", "marketing_start_date": "20190801"}, {"sample": false, "description": "1041000 mL in 1 CONTAINER (65601-801-99)", "package_ndc": "65601-801-99", "marketing_start_date": "20210701"}], "brand_name": "Advanced Alcohol Gel Sanitizer", "product_id": "65601-801_4b08e38b-43e8-1e6d-e063-6394a90a6422", "dosage_form": "GEL", "product_ndc": "65601-801", "generic_name": "Alcohol", "labeler_name": "Betco Corporation, Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Alcohol Gel Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190801", "listing_expiration_date": "20271231"}