SMART CARE LUXURY HAND SANITIZER MIDNIGHT MUSK- alcohol spray

Smart Care Luxury Hand Sanitizer Midnight Musk by

Drug Labeling and Warnings

Smart Care Luxury Hand Sanitizer Midnight Musk by is a Otc medication manufactured, distributed, or labeled by LANTERN HEALTH & BEAUTY SDN. BHD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Active ingredient ... Purpose
Ethyl Alcohol 70% v/v...Antiseptic

Uses

Decreases bacteria on skin.

Warning

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

when using this product

Do not get into eyes. If contact occurs, rinse thoroughly with water.

Do not use

If you are allergic to any of the ingredients.

stop use and ask a doctor

If irritation or rash develops and continues for more than 72 hours.

keep out of reach of children

If swallowed get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 6 years and older
Spray onto hands and rub them together until dry.
Recommended for repeated use.
Children under 6 year of age
Should be supervised when using this product.

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Gel, Aminomethyl Propanol, Blue 1, Denatonium Benzoate, Fragrance, Glycerin, Peg-40 Hydrogenated Castor Oil, Red 4, Tocopheryl Acetate, Watre, Yeiiow 5.

other Information

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

Questions or comments?

Call toll free 1-877-274-8358

packing

packing

INGREDIENTS AND APPEARANCE

SMART CARE LUXURY HAND SANITIZER MIDNIGHT MUSK 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87016-002
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87016-002-01	40 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/14/2025

Labeler - LANTERN HEALTH & BEAUTY SDN. BHD. (965347592)

Establishment
Name	Address	ID/FEI	Business Operations
LANTERN HEALTH & BEAUTY SDN. BHD.		965347592	manufacture(87016-002)