HAND SANITIZER- ethyl alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Ethyl Alcohol 70%

PURPOSE

Antiseptic

INDICATIONS & USAGE

Uses：

Hand sanitizer can help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

Warnings:

For external use only. Flammable.

Keep away from heat or flame.

DO NOT USE

Do not use：

• In children less than 2 months of age.
• On open skin wounds.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Surpervise children under 6 years of age when using this product to avoid swallowing.

OTHER SAFETY INFORMATION

Other info:

• Store between 15-30℃（59-86℉）
• Avoid freezing and excessive heat above 40℃（104℉）

INACTIVE INGREDIENT

Inactive Ingredients:

Ethyl Alcohol, Water, Glycerin, Propylene glycol, Propanediol, Tocopheryl acetate, Aloe barbadensis leaf juice, Aminomethyl propanol, Simmondsia chinensis (jojoba) seed oil, Helianthus annuus (sunflower) seed oil, Vaccinium macrocarpon (cranberry) fruit extract, Punica granatum extract, Vaccinium angustifolium (blueberry) fruit extract, Fragaria chiloensis ( strawberry) fruit extract, Actinidia chinesis (kiwi) fruit extract.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47993-296
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 112 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPANEDIOL (UNII: 5965N8W85T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
JOJOBA OIL (UNII: 724GKU717M)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CRANBERRY JUICE (UNII: Y74M3X3345)
PUNICA GRANATUM LEAF (UNII: O9486I5JXI)
VACCINIUM ANGUSTIFOLIUM LEAF (UNII: B4L873GNG1)
FRAGARIA VESCA LEAF (UNII: I14FE7JUBB)
KIWI FRUIT (UNII: 71ES77LGJC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47993-296-01	1000 mL in 1 BAG; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020

Labeler - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)

Registrant - NINGBO JIANGBEI OCEAN STAR TRADING CO.,LTD (529334491)