Home DailyMed 3f4138df-6903-31e9-e054-00144ff88e88 HAND SANITIZER Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer NingBo Huize Commodity Co.,Ltd.
Effective date 2018-01-06
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-05-31 22:53:59 Label at a glance# Product HAND SANITIZER
Active ingredient ALCOHOL
Label structure 7 sections
Dosage and administration Squeeze ont oh ands and rub hands and rub hands together briskly until dry Can be used anytime any place, without water or towels Contains moisturizers and vitamin E to leave hands feeling refreshed ,soft and smooth without stickiness or residue.
DailyMed RxNorm Mappings# RxCUI, RxNorm string, TTY table RxCUI RxNorm string TTY SPL version 581660 ethanol 62 % Topical Gel PSN 2 581660 ethanol 0.62 ML/ML Topical Gel SCD 2 581660 ethanol 62 % Topical Gel SY 2
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71011-001-01 HAND SANITIZER 5 mL in 1 BOTTLE, PLASTIC GEL 5 2 71011-001-02 HAND SANITIZER 8 mL in 1 BOTTLE, PLASTIC GEL 8 2 71011-001-03 HAND SANITIZER 10 mL in 1 BOTTLE, PLASTIC GEL 10 2 71011-001-04 HAND SANITIZER 15 mL in 1 BOTTLE, PLASTIC GEL 15 2 71011-001-05 HAND SANITIZER 20 mL in 1 BOTTLE, PLASTIC GEL 20 2 71011-001-06 HAND SANITIZER 30 mL in 1 BOTTLE, PLASTIC GEL 30 2 71011-001-07 HAND SANITIZER 50 mL in 1 BOTTLE, PLASTIC GEL 50 2 71011-001-08 HAND SANITIZER 60 mL in 1 BOTTLE, PLASTIC GEL 60 2 71011-001-09 HAND SANITIZER 80 mL in 1 BOTTLE, PLASTIC GEL 80 2 71011-001-10 HAND SANITIZER 100 mL in 1 BOTTLE, PLASTIC GEL 100 2 71011-001-11 HAND SANITIZER 150 mL in 1 BOTTLE, PLASTIC GEL 150 2 71011-001-12 HAND SANITIZER 200 mL in 1 BOTTLE, PLASTIC GEL 200 2 71011-001-13 HAND SANITIZER 250 mL in 1 BOTTLE, PLASTIC GEL 250 2 71011-001-14 HAND SANITIZER 300 mL in 1 BOTTLE, PLASTIC GEL 300 2 71011-001-15 HAND SANITIZER 400 mL in 1 BOTTLE, PLASTIC GEL 400 2 71011-001-16 HAND SANITIZER 500 mL in 1 BOTTLE, PLASTIC GEL 500 2 71011-001-17 HAND SANITIZER 600 mL in 1 BOTTLE, PLASTIC GEL 600 2 71011-001-18 HAND SANITIZER 700 mL in 1 BOTTLE, PLASTIC GEL 700 2 71011-001-19 HAND SANITIZER 800 mL in 1 BOTTLE, PLASTIC GEL 800 2 71011-001-20 HAND SANITIZER 900 mL in 1 BOTTLE, PLASTIC GEL 900 2 71011-001-21 HAND SANITIZER 1000 mL in 1 BOTTLE, PLASTIC GEL 1000 2 71011-001-22 HAND SANITIZER 2000 mL in 1 BOTTLE, PLASTIC GEL 2000 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71011-001 HAND SANITIZER (ALCOHOL) GEL [NINGBO HUIZE COMMODITY CO.,LTD.] 2 Legacy NDC, 22 package rows 20180108_3f4138df-6903-31e9-e054-00144ff88e88.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 9 matching rows.
HAND SANITIZER ALCOHOL WATER GLYCERIN TRIETHANOLAMINE DIOLEATE 24-HOMO-1,25-DIHYDROXYVITAMIN D3 ALOE VERA LEAF CARBOMER 934 PROPYLENE GLYCOL DIACETATE NDC Codes# Product NDC, Package NDC table Product NDC Package NDC 71011-001 71011-001-01 , 71011-001-02 , 71011-001-03 , 71011-001-04 , 71011-001-05 , 71011-001-06 , 71011-001-07 , 71011-001-08 , 71011-001-09 , 71011-001-10 , 71011-001-11 , 71011-001-12 , 71011-001-13 , 71011-001-14 , 71011-001-15 , 71011-001-16 , 71011-001-17 , 71011-001-18 , 71011-001-19 , 71011-001-20 , 71011-001-21 , 71011-001-22
Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 8 matching rows.
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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.