Rose Hand Sanitizer

Manufacturer
Sutra Beauty Inc | Guangzhou Joy Claire Biological Technology Co.,Ltd
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:36:05

Label at a glance#

ProductRose Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Aqua, Camellia Sinensis Leaf Oil, Carbomer, Rosmarinus Officinalis (Rosemary) Leaf Oil,
Parfum.

Use

INDICATIONS & USAGE SECTION

  • Hand Sanitizer to help reduce bacteria that can potentially cause disease.
  • For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • On children less than 2 months of age.
  • On open skin wounds.

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F).
  • Avoid freezing and excessive heat above 40C (104F).

Questions or Comments?

OTC - QUESTIONS SECTION

  • Call 1-888-463-6332 Monday-Friday 9AM-5PM EST. FDA NDC Product Code: 76741-005-12

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

120 ml NDC: 76741-005-12

120 mL120 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN3
1047755ethanol 0.75 ML/ML Topical SolutionSCD3
1047755ethanol 75 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76741-005-122022-01-28C16284748780-1d6a99b39-815b-a426-e053-dadaa90af4c2af489ea1-14c0-33f0-e053-2995a90abdd1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76741-005-12Rose Hand Sanitizer120 mL in 1 BOTTLE, DISPENSINGSOLUTION1203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76741-005ROSE HAND SANITIZER (ETHYL ALCOHOL) SOLUTION [SUTRA BEAUTY INC]3Legacy NDC, 1 package rows20201230_af489ea1-14c0-33f0-e053-2995a90abdd1.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
76741-00576741-005-12

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
b7a2198b-c717-41b8-e053-2995a90aa07daf489ea1-14c0-33f0-e053-2995a90abdd12020-12-29WarningsExact identifier
spl id: b7a2198b-c717-41b8-e053-2995a90aa07d
spl set id: af489ea1-14c0-33f0-e053-2995a90abdd1

Reported adverse events (FAERS/openFDA)#

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