thompson hand sanitizer
Generic: alcohol gel
Labeler: thompsonDrug Facts
Product Profile
Brand Name
thompson hand sanitizer
Generic Name
alcohol gel
Labeler
thompson
Dosage Form
GEL
Routes
Active Ingredients
alcohol 540.26 g/L
Manufacturer
Identifiers & Regulatory
Product NDC
73408-513
Product ID
73408-513_3e4f91aa-aee1-f154-e063-6394a90a951d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2023-10-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73408513
Hyphenated Format
73408-513
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
thompson hand sanitizer (source: ndc)
Generic Name
alcohol gel (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 540.26 g/L
Packaging
- 25 PACKET in 1 BOX (73408-513-73) / .00168 L in 1 PACKET
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3e4f91aa-aee1-f154-e063-6394a90a951d", "openfda": {"upc": ["0073408511737"], "unii": ["3K9958V90M"], "spl_set_id": ["06beaf35-f814-bf9b-e063-6294a90aec8c"], "manufacturer_name": ["Thompson"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 PACKET in 1 BOX (73408-513-73) / .00168 L in 1 PACKET", "package_ndc": "73408-513-73", "marketing_start_date": "20231002"}], "brand_name": "Thompson Hand Sanitizer", "product_id": "73408-513_3e4f91aa-aee1-f154-e063-6394a90a951d", "dosage_form": "GEL", "product_ndc": "73408-513", "generic_name": "alcohol gel", "labeler_name": "Thompson", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thompson Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "540.26 g/L"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231002", "listing_expiration_date": "20261231"}