aruba aloe hand sanitizer
Generic: alcohol
Labeler: aruba aloe balm nvDrug Facts
Product Profile
Brand Name
aruba aloe hand sanitizer
Generic Name
alcohol
Labeler
aruba aloe balm nv
Dosage Form
CREAM
Routes
Active Ingredients
alcohol 80 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
53675-213
Product ID
53675-213_3bc6d7a9-3a5b-92eb-e063-6294a90a5a37
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-06-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53675213
Hyphenated Format
53675-213
Supplemental Identifiers
UPC
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
aruba aloe hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mL/100mL
Packaging
- 59 mL in 1 TUBE (53675-213-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3bc6d7a9-3a5b-92eb-e063-6294a90a5a37", "openfda": {"upc": ["0082252054000"], "unii": ["3K9958V90M"], "spl_set_id": ["3bc6d696-43d2-9516-e063-6294a90ae82b"], "manufacturer_name": ["Aruba Aloe Balm NV"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 TUBE (53675-213-00)", "package_ndc": "53675-213-00", "marketing_start_date": "20250615"}], "brand_name": "Aruba Aloe Hand Sanitizer", "product_id": "53675-213_3bc6d7a9-3a5b-92eb-e063-6294a90a5a37", "dosage_form": "CREAM", "product_ndc": "53675-213", "generic_name": "ALCOHOL", "labeler_name": "Aruba Aloe Balm NV", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aruba Aloe Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "80 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250615", "listing_expiration_date": "20261231"}