BeautyTreats HAND SANITIZER

Manufacturer
Zhejiang Yiwu Limei Cosmetics Co., Ltd
Effective date
2020-05-31
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-05-31 23:15:28

Label at a glance#

ProductBeautyTreats HAND SANITIZER
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

spray directly on hands and rub thoroughly for children under 6 , use only with adult supervision. Not recommended for infants.

Storage and handling

Store below 110F (43F) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NA

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin, Recommended repeated use..

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 directly on hands and rub thoroughly
  • for children under 6 , use only with adult supervision. Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F (43F)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 mL NDC: 74765-015-01 50ml50ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN16
2286295ethanol 0.75 ML/ML Topical SpraySCD16
2286295ethanol 75 % Topical SpraySY16

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74765-015-012022-01-28C16284748780-1d6a99b39-5876-a426-e053-dadaa90af4c2a55be250-f75b-8431-e053-2995a90a19a3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74765-015-01BeautyTreats HAND SANITIZER59 mL in 1 BOTTLE, SPRAYSPRAY5916

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74765-015BEAUTYTREATS HAND SANITIZER (ALCOHOL) SPRAY [ZHEJIANG YIWU LIMEI COSMETICS CO., LTD]16Legacy NDC, 1 package rows20200601_a55be250-f75b-8431-e053-2995a90a19a3.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74765-01574765-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
a6fbfbd2-8fcc-abfb-e053-2a95a90a1310a55be250-f75b-8431-e053-2995a90a19a32020-05-31WarningsExact identifier
spl id: a6fbfbd2-8fcc-abfb-e053-2a95a90a1310
spl set id: a55be250-f75b-8431-e053-2995a90a19a3

Reported adverse events (FAERS/openFDA)#

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