hand sanitizer
Generic: hand sanitizer
Labeler: fehr bros. industries incDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
hand sanitizer
Labeler
fehr bros. industries inc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 67 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
83038-693
Product ID
83038-693_28c533c1-0cfa-d184-e063-6294a90aeb64
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-03-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83038693
Hyphenated Format
83038-693
Supplemental Identifiers
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
hand sanitizer (source: ndc)
Generic Name
hand sanitizer (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 67 mL/100mL
Packaging
- 118 mL in 1 BOTTLE, PLASTIC (83038-693-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "28c533c1-0cfa-d184-e063-6294a90aeb64", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["eac3f46a-1b61-c4b2-e053-2995a90ae702"], "manufacturer_name": ["Fehr Bros. Industries Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, PLASTIC (83038-693-01)", "package_ndc": "83038-693-01", "marketing_start_date": "20200310"}], "brand_name": "Hand Sanitizer", "product_id": "83038-693_28c533c1-0cfa-d184-e063-6294a90aeb64", "dosage_form": "LIQUID", "product_ndc": "83038-693", "generic_name": "Hand Sanitizer", "labeler_name": "Fehr Bros. Industries Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "67 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200310", "listing_expiration_date": "20261231"}