antibacterial hand sanitizer
Generic: alcohol
Labeler: tekweld incDrug Facts
Product Profile
Brand Name
antibacterial hand sanitizer
Generic Name
alcohol
Labeler
tekweld inc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 62 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
71160-188
Product ID
71160-188_0ec200c0-eac3-08fb-e063-6294a90a2fde
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2024-02-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71160188
Hyphenated Format
71160-188
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
antibacterial hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 62 mL/100mL
Packaging
- 12 mL in 1 BOTTLE (71160-188-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0ec200c0-eac3-08fb-e063-6294a90a2fde", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["247835"], "spl_set_id": ["f8dcfaed-9b3d-4c7a-a93e-407c7f62051f"], "manufacturer_name": ["TEKWELD INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 mL in 1 BOTTLE (71160-188-12)", "package_ndc": "71160-188-12", "marketing_start_date": "20240215"}], "brand_name": "Antibacterial Hand Sanitizer", "product_id": "71160-188_0ec200c0-eac3-08fb-e063-6294a90a2fde", "dosage_form": "LIQUID", "product_ndc": "71160-188", "generic_name": "ALCOHOL", "labeler_name": "TEKWELD INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}