APOLLO INSTANT HAND SANITIZER- instant hand sanitizer gel

apollo Instant Hand Sanitizer by

Drug Labeling and Warnings

apollo Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sbu Group L.P., GUANGZHOU XUELEI COSMETIC CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Alcohol 75%

Purpose

Antiseptic

Uses:

Hand sanitizer to help decrease bacterial on the skin, when water, soap& towel are not available. Recommended for repeated use.

Warnings

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

Do not apply around eyes. Do not use in ears & mouth.

WHEN USING

When using this product,

Avoid contact with eyes. In case of contact flush eyes with water.

STOP USE

Stop use and ask a doctor

If redness or irritation develop and persist for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Children must be supervised in use of this product.

Directions

Place enough product into your palms and thoroughly spread on both hands. Rub into skin until dry.

Other information

Store below 110℉（43℃）

May discolor certain fabrics or surfaces.

Inactive ingredients

Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, Propylene Glycol, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Power, Lactic Acid, Citric Acid.

PDP

3785ml NDC: 74658-009-01

INGREDIENTS AND APPEARANCE

APOLLO INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78303-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LINALOOL, (+/-)- (UNII: D81QY6I88E)
3-HEXENYL ACETATE, (3Z)- (UNII: 6INA6GC5I6)
3-HEXEN-1-OL, (3Z)- (UNII: V14F8G75P4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
NEROL (UNII: 38G5P53250)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E)
LACTIC ACID (UNII: 33X04XA5AT)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78303-002-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/02/2020

Labeler - Sbu Group L.P. (841530095)

Registrant - GUANGZHOU XUELEI COSMETIC CO.,LTD. (526885026)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGZHOU XUELEI COSMETIC CO.,LTD.		526885026	manufacture(78303-002) , pack(78303-002) , label(78303-002)