candy cutie hand sanitizer
Generic: alcohol
Labeler: target corporationDrug Facts
Product Profile
Brand Name
candy cutie hand sanitizer
Generic Name
alcohol
Labeler
target corporation
Dosage Form
GEL
Routes
Active Ingredients
alcohol .62 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-074
Product ID
11673-074_0896ba3c-9eee-2fc2-e063-6394a90a2d29
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673074
Hyphenated Format
11673-074
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
candy cutie hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .62 mL/mL
Packaging
- 30 mL in 1 BOTTLE (11673-074-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0896ba3c-9eee-2fc2-e063-6394a90a2d29", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["920d0dc5-2803-4a25-8f1f-86d7ff61c568"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (11673-074-00)", "package_ndc": "11673-074-00", "marketing_start_date": "20200501"}], "brand_name": "candy cutie hand sanitizer", "product_id": "11673-074_0896ba3c-9eee-2fc2-e063-6394a90a2d29", "dosage_form": "GEL", "product_ndc": "11673-074", "generic_name": "ALCOHOL", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "candy cutie hand sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}