HAND SANITIZER MIST- ethyal 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%

PURPOSE

ANTISEPTIC

INDICATIONS & USAGE

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

WARNINGS

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

DO NOT USE

Redness of irritation develop.
Condition persists for more than 72 hours.

WHEN USING

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.

DOSAGE & ADMINISTRATION

Spray product in your palm and rub hands together until dry.
For children under 6, use only under adult supervision.
Not recommended for infants.

STORAGE AND HANDLING

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

INACTIVE INGREDIENT

Water, Glycerin, Dipropylene Glycol, Glycereth-26, Fragrance, Butylene Glycol, Leuconostoc/Radish Root Ferment Filtrate, Aloe Barbadensis Leaf Juice, Phenoxyethanol.

May Contain:Red 40 Lake (CI 16035),Red 33 Lake (CI 17200),Red 4 Lake(CI 14700),Yellow 5 Lake(CI 19140:1),Blue 1 Lake (CI 42090:2).

KEEP OUT OF REACH OF CHILDREN

Children should be supervised by an adult when using this product.
lf swallowed, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER MIST 
ethyal alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85472-005
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)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERETH-26 (UNII: NNE56F2N14)
GLYCERIN (UNII: PDC6A3C0OX)
RED 40 LAKE (UNII: 6T47AS764T)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
BLUE 1 LAKE (UNII: J9EQA3S2JM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85472-005-01	40 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/24/2025
2	NDC: 85472-005-02	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/24/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/24/2025

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

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG GAORONG COSMETIC CO.,LTD.		421318550	manufacture(85472-005)