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.
Recommended for repeated use.

Warning

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

Keep out of eyes, in case of contact with eyes, flush

thoroughly with water.

Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children.In case of ingestion, seek

medical help or contact a Poison Control Center right away.

WHEN USING

none

STOP USE

Stop use and ask a doctor if skin irritation develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of ingestion, seek
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 Lake(Cl 14700),Yellow 5 Lake(Cl19140),Red 33 Lake(C117200),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: 85472-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERETH-26 (UNII: NNE56F2N14)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
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: 85472-002-01	40 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(85472-002)