e2 sanitizing hand

Generic: e2 sanitizing hand

Labeler: kutol products company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name e2 sanitizing hand
Generic Name e2 sanitizing hand
Labeler kutol products company
Dosage Form SOAP
Routes
TOPICAL
Active Ingredients

benzalkonium chloride .003 mg/mL

Manufacturer
KUTOL PRODUCTS COMPANY

Identifiers & Regulatory

Product NDC 50865-017
Product ID 50865-017_298f1da8-676b-6cb9-e063-6294a90a78ab
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2015-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50865017
Hyphenated Format 50865-017

Supplemental Identifiers

UPC
0686702017074 0686702017098
UNII
F5UM2KM3W7

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 e2 sanitizing hand (source: ndc)
Generic Name e2 sanitizing hand (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .003 mg/mL
source: ndc
Packaging
  • 209000 mL in 1 DRUM (50865-017-03)
  • 4000 mL in 1 BOTTLE, PLASTIC (50865-017-07)
  • 4000 mL in 1 BOTTLE, PLASTIC (50865-017-09)
  • 1000 mL in 1 BAG (50865-017-41)
  • 800 mL in 1 BAG (50865-017-65)
  • 2000 mL in 1 BOTTLE, PLASTIC (50865-017-67)
source: ndc

Packages (6)

50865-017-03 209000 mL in 1 DRUM (50865-017-03) 50865-017-07 4000 mL in 1 BOTTLE, PLASTIC (50865-017-07) 50865-017-09 4000 mL in 1 BOTTLE, PLASTIC (50865-017-09) 50865-017-41 1000 mL in 1 BAG (50865-017-41) 50865-017-65 800 mL in 1 BAG (50865-017-65) 50865-017-67 2000 mL in 1 BOTTLE, PLASTIC (50865-017-67)

Ingredients (1)

benzalkonium chloride (.003 mg/mL)

Linked Drug Pages (1)

E2 SANITIZING HAND ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "298f1da8-676b-6cb9-e063-6294a90a78ab", "openfda": {"upc": ["0686702017074", "0686702017098"], "unii": ["F5UM2KM3W7"], "spl_set_id": ["70357eaf-8cd8-4c5e-b7a8-ae2fbba0ca2e"], "manufacturer_name": ["KUTOL PRODUCTS COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "209000 mL in 1 DRUM (50865-017-03)", "package_ndc": "50865-017-03", "marketing_start_date": "20150915"}, {"sample": false, "description": "4000 mL in 1 BOTTLE, PLASTIC (50865-017-07)", "package_ndc": "50865-017-07", "marketing_start_date": "20150915"}, {"sample": false, "description": "4000 mL in 1 BOTTLE, PLASTIC (50865-017-09)", "package_ndc": "50865-017-09", "marketing_start_date": "20150915"}, {"sample": false, "description": "1000 mL in 1 BAG (50865-017-41)", "package_ndc": "50865-017-41", "marketing_start_date": "20150915"}, {"sample": false, "description": "800 mL in 1 BAG (50865-017-65)", "package_ndc": "50865-017-65", "marketing_start_date": "20150915"}, {"sample": false, "description": "2000 mL in 1 BOTTLE, PLASTIC (50865-017-67)", "package_ndc": "50865-017-67", "marketing_start_date": "20150915"}], "brand_name": "E2 SANITIZING HAND", "product_id": "50865-017_298f1da8-676b-6cb9-e063-6294a90a78ab", "dosage_form": "SOAP", "product_ndc": "50865-017", "generic_name": "E2 SANITIZING HAND", "labeler_name": "KUTOL PRODUCTS COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "E2 SANITIZING HAND", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".003 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150915", "listing_expiration_date": "20261231"}