MARY KAY SATIN HANDS SHEA HAND SANITIZER- alcohol solution

Mary Kay Satin Hands Shea Hand Sanitizer by

Drug Labeling and Warnings

Mary Kay Satin Hands Shea Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Mary Kay Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Alcohol 75% v/v

Purpose

Antiseptic

Uses

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

Warnings

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

Do not use

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

When using this product

keep out of eyes, ears, and mouth.

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

Stop use and ask a doctor

if irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

• 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

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

Inactive ingredients

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

Questions?

Call toll-free 1-800-627-9529

Principal Display Panel - 50 ml carton

Mary Kay

Satin Hands Shea Hand Sanitizer

Fragrance-Free

1.7 FL. OZ. / 50 ml

INGREDIENTS AND APPEARANCE

MARY KAY SATIN HANDS SHEA HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51531-8735
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BETAINE (UNII: 3SCV180C9W)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-50 SHEA BUTTER (UNII: SF35CE4XLR)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51531-8735-7	1 in 1 CARTON	11/16/2020
1		50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/16/2020

Labeler - Mary Kay Inc. (049994452)

Establishment
Name	Address	ID/FEI	Business Operations
Mary Kay Inc.		103978839	manufacture(51531-8735)