BEAUTIMAX HAND SANITIZER

Manufacturer
Huizhou Beautimax Cosmetics Co. LTD
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:16

Label at a glance#

ProductBEAUTIMAX HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

/

Storage and handling

store in cooldry place dont store ahoye., may discolor somefabrics.humanfulto wood and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Non-medical For extemmaland dally use only. Stop use and ask a doctor imitation and redness develop,. Keep out reach of children, If get into eyes,rinse eyesthroughly with water If swallowed, get medical help or ask.

Do not use

OTC - DO NOT USE SECTION

  • Stop use and ask a doctor imitation and redness develop

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use and ask a doctor imitation and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out reach of children, If get into eyes,rinse eyesthroughly with water If swallowed, get medical help or ask..

Directions

DOSAGE & ADMINISTRATION SECTION

/

Other information

STORAGE AND HANDLING SECTION

store in cooldry place dont store ahoye., may discolor somefabrics.humanfulto wood and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua, Glycerin, PropyleneGlycol, Acrylates/C10-30 Alkyl Acrylate CrosspolymetFragrance/Parfum, Aloe Barbadensis Leaf ExtractDisodium EDTA

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

223344

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76715-006-012022-01-28C16284748780-1d6a99b39-d9c2-a426-e053-dadaa90af4c2HAND SANITIZER
76715-006-022022-01-28C16284748780-1d6a99b39-d9c2-a426-e053-dadaa90af4c2HAND SANITIZER
76715-006-032022-01-28C16284748780-1d6a99b39-d9c2-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76715-006-01BEAUTIMAX HAND SANITIZER60 mL in 1 BOTTLEGEL601
76715-006-02BEAUTIMAX HAND SANITIZER100 mL in 1 BOTTLEGEL1001
76715-006-03BEAUTIMAX HAND SANITIZER500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76715-006BEAUTIMAX HAND SANITIZER (HAND SANITIZER) GEL [HUIZHOU BEAUTIMAX COSMETICS CO. LTD]1Legacy NDC, 3 package rows20200516_a5961726-b657-ac6d-e053-2995a90af8f7.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76715-00676715-006-01, 76715-006-02, 76715-006-03

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
a5962233-e6ff-3491-e053-2995a90a5287a5961726-b657-ac6d-e053-2995a90af8f72020-05-14WarningsExact identifier
spl id: a5962233-e6ff-3491-e053-2995a90a5287
spl set id: a5961726-b657-ac6d-e053-2995a90af8f7

Reported adverse events (FAERS/openFDA)#

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