WISH HAND SANITIZER BLACK PLUM VANILLA- alcohol hand sanitizer spray

WISH HAND SANITIZER BLACK PLUM VANILLA by

Drug Labeling and Warnings

WISH HAND SANITIZER BLACK PLUM VANILLA by is a Otc medication manufactured, distributed, or labeled by PT. SUPER HOME PRODUCT INDONESIA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions:

Spray onto hands and rub together until dry. Recommended for repeat use.Children under 6 years of age should be supervised when using this product

Inactive Ingredients:

Water(Aqua), Glycerin,Aminomethyl Propanol,Fragrance,Aloe Barbadensis Leaf Juice,Tocopheryl Acetate(Vitamin E),Yellow 6,Red 40.

Warnings:

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

When using this product:

In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor if:

lrritation and redness occurs.

Keep out of reach of children:

lf swallowed, get medical help or contact a Poison Control Center.

Active Ingredients:

Ethyl Alcohol 70% v/v Purpose：Antimicrobial

USE

Hand sanitizer helps reduce bacteria and the spread of germs.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WISH HAND SANITIZER BLACK PLUM VANILLA 
alcohol hand sanitizer spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85537-103
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.005 mL  in 100 mL
AQUA (UNII: 059QF0KO0R)	25.9 mL  in 100 mL
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.001 mL  in 100 mL
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)	0.0005 mL  in 100 mL
FD&C RED NO. 40 (UNII: WZB9127XOA)	0.0005 mL  in 100 mL
PLUM (UNII: 67M3EQ6BE1)	2 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)	0.093 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85537-103-01	35 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	04/23/2025

Labeler - PT. SUPER HOME PRODUCT INDONESIA (564862692)

Registrant - PT. SUPER HOME PRODUCT INDONESIA (564862692)

Establishment
Name	Address	ID/FEI	Business Operations
PT. SUPER HOME PRODUCT INDONESIA		564862692	manufacture(85537-103)