ANTI-BACTERIAL HAND SANITIZER GEL- ethyl alcohol gel

Anti-Bacterial Hand Sanitizer Gel by

Drug Labeling and Warnings

Anti-Bacterial Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Ningbo Riway Daily Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Ethyl Alcohol 75%.

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria 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 this product, avoid contact with eyes.
In case of contact flush eyes with water.
Stop use and ask a doctor it 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

Squeeze the bottle after removing the lid and thoroughly spread on both hands. Rub into skin until dry.

Other information

Store at 20 °C(88 to 77°F) may discolor fabrices.

Inactive ingredients

Water,Glycerin, Aloe barbadensis leaf extract,Carbomer,Tocopheryl Acetate,Triethanolamine.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ANTI-BACTERIAL HAND SANITIZER GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77267-004
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
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77267-004-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/23/2020
2	NDC: 77267-004-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/23/2020
3	NDC: 77267-004-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/23/2020
4	NDC: 77267-004-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/23/2020
5	NDC: 77267-004-05	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/23/2020

Labeler - Ningbo Riway Daily Commodity Co., Ltd (540997562)

Registrant - Ningbo Riway Daily Commodity Co., Ltd (540997562)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Riway Daily Commodity Co., Ltd		540997562	manufacture(77267-004)