HAND SANITIZER MIST- ethyl alcohol spray

Hand Sanitizer Mist by

Drug Labeling and Warnings

Hand Sanitizer Mist by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG GAORONG COSMETIC CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ETHYL ALCOHOL 70%

USE

To decrease bacteria on the skin that could cause disease.
When water, soap and towel are not available.
Recommended for repeated use.

Warning

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

When using this product：

Keep out of eyes, ears, or mouth.

In case of eye contact, flush eyes thoroughly with water.

Avoid contact with broken skin.

Do not inhale or ingest.

Stop use and ask a doctor if

Redness of irritation develop

Condition persists for more than 72 hours

Keep out of reach of children

Children should be supervised by an adult when using this product.

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

Purpose

ANTISEPTIC

Other information

Do not store above 105°F.
May discolor some fabrics
Harmful to wood finishes and plastics.

Directions

Spary product in your palm and rub hands together until dry.

For children under 6, use only under adult supervision

Not recommended for infants

Inactive Ingredients

Water, Glycerin, Dipropylene Glycol, Glycereth-26,Fragrance, Butylene Glycol, Leuconostoc Radish RootFerment Filtrate, Aloe Barbadensis Leaf Juice,Phenoxyethanol. May Contain: Red 4(Cl 14700),Yellow 5(Cl19140),Red 40(C116035)Red 33(C117200),Red 28(Cl45410),Blue 1(Cl 42090)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER MIST 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85472-001
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)
GLYCERETH-26 (UNII: NNE56F2N14)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
D&C RED NO. 28 (UNII: 767IP0Y5NH)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85472-001-01	40 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025
2	NDC: 85472-001-02	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/01/2025

Labeler - ZHEJIANG GAORONG COSMETIC CO.,LTD. (421318550)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG GAORONG COSMETIC CO.,LTD.		421318550	manufacture(85472-001)