Mary Kay Satin Hands Shea Hand Sanitizer

Manufacturer
Mary Kay Inc.
Effective date
2024-12-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:47:48

Label at a glance#

ProductMary Kay Satin Hands Shea Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

Spray 3+ pumps on hands, insuring both are thoroughly covered. Rub hands together briskly until dry. Supervise children under 6 years of age when using this product.

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria
on the skin. For use when soap and water
are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep
away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth.

In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact
a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray 3+ pumps on hands, insuring both are thoroughly covered. Rub hands together briskly until dry.
  • Supervise children under 6 years of age when using this product.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, betaine,
butylene glycol, glycerin, peg-50 shea
butter, phenoxyethanol, water

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-627-9529

Principal Display Panel - 50 ml carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mary Kay

Satin Hands Shea Hand Sanitizer

Fragrance-Free

1.7 FL. OZ. / 50 ml

Image of Hand Sanitizer CartonImage of Hand Sanitizer Carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51531-8735-7Mary Kay Satin Hands Shea Hand Sanitizer50 mL in 1 BOTTLE, SPRAYSOLUTION502
51531-8735-7Mary Kay Satin Hands Shea Hand Sanitizer1 in 1 CARTONSOLUTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51531-8735MARY KAY SATIN HANDS SHEA HAND SANITIZER (ALCOHOL) SOLUTION [MARY KAY INC.]2Current NDC, Legacy NDC, 2 package rows20241222_b6c2b979-2940-1569-e053-2995a90a532c.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
51531-873551531-8735-7

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

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
Mary Kay Satin Hands Shea Hand SanitizerALCOHOLMary Kay Inc.b6c2b979-2940-1569-e053-2995a90a532c2024-12-17WarningsExact identifier
ndc (package): 51531-8735-7
ndc (product): 51531-8735
ndc11 (package): 51531873507
spl id: 297cd44b-d36c-47a2-e063-6394a90ae948
spl set id: b6c2b979-2940-1569-e053-2995a90a532c

Reported adverse events (FAERS/openFDA)#

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