lavender life hand sanitizer
Generic: alcohol
Labeler: target corporationDrug Facts
Product Profile
Brand Name
lavender life hand sanitizer
Generic Name
alcohol
Labeler
target corporation
Dosage Form
GEL
Routes
Active Ingredients
alcohol 620 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
11673-861
Product ID
11673-861_08996402-654d-a52c-e063-6294a90afcd7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2019-05-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673861
Hyphenated Format
11673-861
Supplemental Identifiers
RxCUI
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
lavender life hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 620 mg/g
Packaging
- 30 g in 1 BOTTLE (11673-861-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "08996402-654d-a52c-e063-6294a90afcd7", "openfda": {"upc": ["0490370851591"], "unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["df0a3166-1658-490c-b3a8-c226040e5220"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 BOTTLE (11673-861-30)", "package_ndc": "11673-861-30", "marketing_start_date": "20190507"}], "brand_name": "lavender life hand sanitizer", "product_id": "11673-861_08996402-654d-a52c-e063-6294a90afcd7", "dosage_form": "GEL", "product_ndc": "11673-861", "generic_name": "ALCOHOL", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "lavender life hand sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "620 mg/g"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}