hand sanitizer

Generic: ethyl alcohol

Labeler: uplift brands, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name hand sanitizer
Generic Name ethyl alcohol
Labeler uplift brands, llc
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

alcohol .62 mL/mL

Manufacturer
UpLift Brands, LLC

Identifiers & Regulatory

Product NDC 83986-721
Product ID 83986-721_4cc534e5-aec3-57f0-e063-6394a90acf72
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2024-04-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83986721
Hyphenated Format 83986-721

Supplemental Identifiers

UNII
3K9958V90M

Packaging Origin

Original Packager
true

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 ethyl alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .62 mL/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, SPRAY (83986-721-20)
source: ndc

Packages (1)

83986-721-20 59 mL in 1 BOTTLE, SPRAY (83986-721-20)

Ingredients (1)

alcohol (.62 mL/mL)

Linked Drug Pages (1)

Hand Sanitizer ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4cc534e5-aec3-57f0-e063-6394a90acf72", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["fbfa510c-2cc8-4ac8-95fc-5ac0a2e570ad"], "manufacturer_name": ["UpLift Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, SPRAY (83986-721-20)", "package_ndc": "83986-721-20", "marketing_start_date": "20240426"}], "brand_name": "Hand Sanitizer", "product_id": "83986-721_4cc534e5-aec3-57f0-e063-6394a90acf72", "dosage_form": "SPRAY", "product_ndc": "83986-721", "generic_name": "Ethyl Alcohol", "labeler_name": "UpLift Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240426", "listing_expiration_date": "20271231"}