Hand Sanitizer Spray

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 00:55:23

Label at a glance#

ProductHand Sanitizer 2oz
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

Store at room temperature may discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands. Flammable, keep away from fire or flame

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rednees develp 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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature
  • may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, aloe barbadensis leaf juice, tocopheryl acetate,

OTC - QUESTIONS SECTION

1-855-345-5575

OTC - WHEN USING SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN2
1041849ethanol 0.7 ML/ML Topical SpraySCD2
1041849ethanol 70 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-132-012025-02-13C16284748780-12cef2736-adff-d83d-e063-dadaa90ab31fHand Sanitizer Spray
57337-132-012025-01-30C16284748780-12cef2736-adff-d83d-e063-dadaa90ab31fHand Sanitizer Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-132-01Hand Sanitizer2oz59 mL in 1 BOTTLE, SPRAYSPRAY592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-132HAND SANITIZER 2OZ (ALCOHOL) SPRAY [NINGBO REJOICE INTERNATIONAL]2Current NDC, Legacy NDC, 1 package rows20250216_b08fd11a-48e2-67b6-e053-2995a90ac399.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57337-13257337-132-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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 2ozALCOHOLNingbo Rejoice Internationalb08fd11a-48e2-67b6-e053-2995a90ac3992025-02-13WarningsExact identifier
ndc (package): 57337-132-01
ndc (product): 57337-132
ndc11 (package): 57337013201
spl id: 2e124c04-24d1-e6dd-e063-6294a90ada2d
spl set id: b08fd11a-48e2-67b6-e053-2995a90ac399

Reported adverse events (FAERS/openFDA)#

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