Home NDC 85782-001-01 Stone Hand Sanitizer
Product NDC 85782-001
Requested package NDC 85782-001-01
11-digit product format 857820001
Labeler code 85782
Product ID 85782-001_3c941aa4-c499-4245-e063-6394a90a0ba2
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler handetizer, LLC.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-17
Substance ISOPROPYL ALCOHOL
Active strength 72 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Stone Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 72 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ND2M416302 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2717558 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85782-001-01 Stone Hand Sanitizer 20 mL in 1 BOTTLE, SPRAY SPRAY 20 2
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85782-001-01 85782000101 20 mL in 1 BOTTLE, SPRAY (85782-001-01) 20 ml 2025-08-17 No No Current