M. SKIN CARE GEL HAND SANITIZER- hand sanitizer gel

M. Skin Care Gel Hand Sanitizer by

Drug Labeling and Warnings

M. Skin Care Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Palm Beach Beaute, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Store at room temperature 20*. 25°C (66*F-77*F)

INACTIVE INGREDIENT

Aqua, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Tocopheryl Acetate, Jojoba Wax PEG-120 Esters, Aloe Barbadensis Leaf Extract, Citric Acid, Sodium Benzoate, Potassium Sorbate, Sodium Sulfite, CI 60730, CI 17200, ISO E SUPER, HEDIONE, DIPROPYLENE GLYCOL, GALAXOLIDE, ETHYLENE BRASSILATE.

INDICATIONS & USAGE

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry.No rinsing required No towels needed.Do not use other than directed.

ACTIVE INGREDIENT

Alcohol

KEEP OUT OF REACH OF CHILDREN

keep out of children

PURPOSE

Disinfection
Sterilization
No Rinseing

WARNINGS

1.Flammable, keep away from fire or fame.
2.For external use only
3.When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
4.Stop use and ask a doctor if redness or iritation or rash appears and persists for more than 72 hours.
5.Keep out of reach of children. If swallowed, get medical help or contact the Poison Control center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

M. SKIN CARE GEL HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77218-002
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	262.5 mL  in 350 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM SULFITE (UNII: VTK01UQK3G)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE (UNII: 1GD7ODM28Y)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77218-002-01	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/24/2020

Labeler - Palm Beach Beaute, LLC (007721815)

Establishment
Name	Address	ID/FEI	Business Operations
Palm Beach Beaute, LLC		007721815	manufacture(77218-002)