VANILLA SKY HAND SANITIZER- alcohol gel

Vanilla Sky Hand Sanitizer by

Drug Labeling and Warnings

Vanilla Sky Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Reaction Retail, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses:

Hand sanitizer to help decrease bacteria on the skin.

Warnings:

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

Stop use and ask doctor 

if irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a doctor right away.

Directions:

Squirt as needed into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other Information:

Store below 118°F.

INACTIVE INGREDIENTS:

Aqua (Water), Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice Parfum (Fragrance) Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Citric Acid, Potassium Sorbate, Sodium Benzoate, Sucrose, Zea Mays (Corn) Starch, Hydroxypropyl Methylcellulose, Polyvinyl Alcohol, Benzyl Benzoate, Hexyl Cinnamal, Limonene, Butylphenyl Methylpropional, Linalool, CI 77267 (D&C Black No.3), CI 60730 (Ext. D&C Violet No.2).

Packgae Labeling:

INGREDIENTS AND APPEARANCE

VANILLA SKY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80026-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
BENZYL BENZOATE (UNII: N863NB338G)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
D&C BLACK NO. 2 (UNII: 4XYU5U00C4)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80026-004-35	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/15/2020

Labeler - Reaction Retail, LLC (968085212)