FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Deqing Jiarou Daily Chemical Co., Ltd
Effective date
2023-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:02:52

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.

Dosage and administration

Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.Children must be supervised in use of this product.

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help decrease bacteria on the skin.
  • When water, soap & towel are not available.
  • Recommended for repeated use.

Warning

WARNINGS SECTION

  • For external use only.
  • Flammable.Keep away from fire or flame.
  • Do not apply around eyes.Do not use in ears & mouth.
  • When using this product, avoid contact with eyes. In case of contact flush eyes with water.
  • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squirt as needed into your palms and thoroughly spread on both hands.
  • Rub into skin until dry.

OTHER SAFETY INFORMATION

  • Store in original container closed.
  • Store at 20°C to 25°C （68°F to 77°F）.
  • May discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Trolamine,Glycerin, carbormer,Tocopherol Acetate, Aloe Vera.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:70675-001-01

10ML10ML

NDC:70675-001-02

15ML15ML

NDC:70675-001-03

20ML20ML

NDC:70675-001-04

30ML30ML

NDC:70675-001-05

50ML50ML

NDC:70675-001-06

60ML60ML

NDC:70675-001-07

100ML100ML

NDC:70675-001-08

120ML120ML

NDC:70675-001-09

240ML240ML

NDC:70675-001-10

500ML500ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN1
247835ethanol 0.62 ML/ML Topical SolutionSCD1
247835ethanol 62 % Topical SolutionSY1
247835ethyl alcohol 62 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70675-001-012025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-022025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-032025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-042025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-052025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-062025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-072025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-082025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-092025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b
70675-001-102025-01-30C16284748780-12cef2736-aea0-d83d-e063-dadaa90ab31f0acc9265-0159-69b1-e063-6294a90a1f1b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70675-001-01HAND SANITIZER10 mL in 1 BOTTLELIQUID101
70675-001-02HAND SANITIZER15 mL in 1 BOTTLELIQUID151
70675-001-03HAND SANITIZER20 mL in 1 BOTTLELIQUID201
70675-001-04HAND SANITIZER30 mL in 1 BOTTLELIQUID301
70675-001-05HAND SANITIZER50 mL in 1 BOTTLELIQUID501
70675-001-06HAND SANITIZER60 mL in 1 BOTTLELIQUID601
70675-001-07HAND SANITIZER100 mL in 1 BOTTLELIQUID1001
70675-001-08HAND SANITIZER120 mL in 1 BOTTLELIQUID1201
70675-001-09HAND SANITIZER240 mL in 1 BOTTLELIQUID2401
70675-001-10HAND SANITIZER500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70675-001HAND SANITIZER (ALCOHOL) LIQUID [DEQING JIAROU DAILY CHEMICAL CO., LTD]110 package rows20231130_0acc9265-0159-69b1-e063-6294a90a1f1b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70675-00170675-001-01, 70675-001-02, 70675-001-03, 70675-001-04, 70675-001-05, 70675-001-06, 70675-001-07, 70675-001-08, 70675-001-09, 70675-001-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0acc9204-e964-42a6-e063-6294a90aae940acc9265-0159-69b1-e063-6294a90a1f1b2023-11-23WarningsExact identifier
spl id: 0acc9204-e964-42a6-e063-6294a90aae94
spl set id: 0acc9265-0159-69b1-e063-6294a90a1f1b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.