advanced hand sanitizer
Generic: ethyl alcohol
Labeler: harris teeterDrug Facts
Product Profile
Brand Name
advanced hand sanitizer
Generic Name
ethyl alcohol
Labeler
harris teeter
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
72036-439
Product ID
72036-439_4a044711-f1be-eacf-e063-6294a90a339b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2014-07-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72036439
Hyphenated Format
72036-439
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
advanced hand sanitizer (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 236 mL in 1 BOTTLE, PUMP (72036-439-34)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4a044711-f1be-eacf-e063-6294a90a339b", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["bb08034b-9516-435a-bbc3-888e9dbaccbf"], "manufacturer_name": ["Harris Teeter"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, PUMP (72036-439-34)", "package_ndc": "72036-439-34", "marketing_start_date": "20140718"}], "brand_name": "Advanced Hand Sanitizer", "product_id": "72036-439_4a044711-f1be-eacf-e063-6294a90a339b", "dosage_form": "GEL", "product_ndc": "72036-439", "generic_name": "Ethyl Alcohol", "labeler_name": "Harris Teeter", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140718", "listing_expiration_date": "20271231"}