FDA.reportPublic FDA data

Hand Sanitizer Vitamin E

Manufacturer
Ningbo Rejoice International | China Ningbo Shangge Technology Co., Ltd.
Effective date
2025-02-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:55:15

Label at a glance#

ProductHand Sanitizer Vitamin E
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0% v/v

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin
  • Recommended for repeated use

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product
  • Briskly rub hands together until dry
  • Supervise children under 6 years in the use of this product

OTHER SAFETY INFORMATION

Other Information

  • store at room temperature
  • may discolor certain fabrics

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer, fragrance, triethanolamine, propylene glycol, tocopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-119-012025-02-13C16284748780-12cef2736-9ff2-d83d-e063-dadaa90ab31f05401#-Hand sanitizer 2X2oz-vitamin E
57337-119-012025-01-30C16284748780-12cef2736-9ff2-d83d-e063-dadaa90ab31f05401#-Hand sanitizer 2X2oz-vitamin E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-119-01Hand Sanitizer Vitamin E59 mL in 1 BOTTLELIQUID592
57337-119-01Hand Sanitizer Vitamin E2 in 1 PACKAGELIQUID22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-119HAND SANITIZER VITAMIN E (ETHYL ALCOHOL) LIQUID [NINGBO REJOICE INTERNATIONAL]2Current NDC, Legacy NDC, 2 package rows20250215_a269a222-95cb-098c-e053-2995a90a21e7.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
57337-11957337-119-01

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
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
Hand Sanitizer Vitamin EETHYL ALCOHOLNingbo Rejoice Internationala269a222-95cb-098c-e053-2995a90a21e72025-02-13WarningsExact identifier
ndc (package): 57337-119-01
ndc (product): 57337-119
ndc11 (package): 57337011901
spl id: 2e0144d7-89d8-7ac8-e063-6394a90a886f
spl set id: a269a222-95cb-098c-e053-2995a90a21e7

Reported adverse events (FAERS/openFDA)#

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