Hand RX Hand Sanitizer

Manufacturer
Yiwu Yangjie Daily Chemicals Co.,Ltd.
Effective date
2020-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:41

Label at a glance#

ProductHand RX Hand Sanitizer
Active ingredientalcohol
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antibacterial

OTC - PURPOSE SECTION

  • decrease bacteria on the skin that could cause disease
  • recommended for repeated use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center right away.

INDICATIONS & USAGE SECTION

Directions:

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommened for infants

WARNINGS SECTION

For external use only - hands
Flammable. Keep away from heat or flame.

When using this product

  • Keep out of eyes. In case of contact with eye, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor

  • skin irritation develops.

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry.

Other Information:

  • do not store above 105℉
  • may discolor some fabrics
  • harmful to wood finished and plastics

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine, Propylene Glycol, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74149-005-012023-01-30C16284748780-1f386c649-f565-0266-e053-dadaa90a7c1aDrug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74149-005-01Hand RX Hand Sanitizer236 mL in 1 BOTTLEGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74149-005HAND RX HAND SANITIZER (ALCOHOL) GEL [YIWU YANGJIE DAILY CHEMICALS CO.,LTD.]1Legacy NDC, 1 package rows20200512_1ad1bade-0124-47e4-aedf-9b7754d6892d.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74149-00574149-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
34b61ac2-2b55-4aed-9967-9bb35ed45d9b1ad1bade-0124-47e4-aedf-9b7754d6892d2020-05-11WarningsExact identifier
spl id: 34b61ac2-2b55-4aed-9967-9bb35ed45d9b
spl set id: 1ad1bade-0124-47e4-aedf-9b7754d6892d

Reported adverse events (FAERS/openFDA)#

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