byotrol hand sanitizer

Generic: benzalkonium chloride

Labeler: advanced hygienics llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name byotrol hand sanitizer
Generic Name benzalkonium chloride
Labeler advanced hygienics llc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1.3 mg/mL

Manufacturer
Advanced Hygienics LLC

Identifiers & Regulatory

Product NDC 63002-002
Product ID 63002-002_ef6a1c09-8491-4a08-bedc-a67ce00d9e23
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part333A
Listing Expiration 2026-12-31
Marketing Start 2014-05-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63002002
Hyphenated Format 63002-002

Supplemental Identifiers

RxCUI
1020365
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 byotrol hand sanitizer (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number part333A (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.3 mg/mL
source: ndc
Packaging
  • 1250 mL in 1 BOTTLE (63002-002-12)
  • 500 mL in 1 BOTTLE (63002-002-50)
  • 9463 mL in 1 BOTTLE (63002-002-75)
  • 50 mL in 1 BOTTLE (63002-002-99)
source: ndc

Packages (4)

Ingredients (1)

benzalkonium chloride (1.3 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "ef6a1c09-8491-4a08-bedc-a67ce00d9e23", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1020365"], "spl_set_id": ["09edbc17-c443-4b0d-9c28-c4b8233c4d1a"], "manufacturer_name": ["Advanced Hygienics LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 BOTTLE (63002-002-12)", "package_ndc": "63002-002-12", "marketing_start_date": "20140625"}, {"sample": false, "description": "500 mL in 1 BOTTLE (63002-002-50)", "package_ndc": "63002-002-50", "marketing_start_date": "20140625"}, {"sample": false, "description": "9463 mL in 1 BOTTLE (63002-002-75)", "package_ndc": "63002-002-75", "marketing_start_date": "20150401"}, {"sample": false, "description": "50 mL in 1 BOTTLE (63002-002-99)", "package_ndc": "63002-002-99", "marketing_start_date": "20140502"}], "brand_name": "Byotrol Hand Sanitizer", "product_id": "63002-002_ef6a1c09-8491-4a08-bedc-a67ce00d9e23", "dosage_form": "LIQUID", "product_ndc": "63002-002", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "Advanced Hygienics LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Byotrol Hand Sanitizer", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "part333A", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20140502", "listing_expiration_date": "20261231"}