DISNEY TOUCHLAND POWER MIST HYDRATING HAND SANITIZER VANILLA BLOSSOM- alcohol spray

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 70% v/v

Purpose

Antiseptic

Uses

• Hand sanitizer to decrease bacteria on the skin.
• Recommended for repeated use.

Warnings

For external use only.
Flammable, keep away from heat or flame.

Do not use

in 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 and rash occurs. These may be signs of serious condition.

Keep out of reach of children.

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

Directions

Spray enough product in your palm to thoroughly cover your hands.
Rub hands together briskly until dry. Recommended for repeated use.
Children under 6 years of age should be supervised when using this product.

Other information

Protect the product in this container from excessive heat and direct sun.
Store below 104°F (40°C).
May discolor certain fabrics.

Inactive ingredients

Water, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Glycereth-26, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Citric Acid, Potassium Sorbate, Sodium Benzoate.

Package Labeling:

INGREDIENTS AND APPEARANCE

DISNEY TOUCHLAND POWER MIST HYDRATING HAND SANITIZER VANILLA BLOSSOM 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72033-155
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
GLYCERETH-26 (UNII: NNE56F2N14)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)
LIME OIL, COLD PRESSED (UNII: UZH29XGA8G)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72033-155-00	1 in 1 CARTON	04/01/2026
1		1 in 1 POUCH
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/01/2026

Labeler - Touchland LLC (036656461)

Registrant - Touchland LLC (036656461)