VERTRA HAND SANITIZER TOPICAL SOLUTION- hand sanitizer topical solution liquid

Vertra Hand Sanitizer topical solution by

Drug Labeling and Warnings

Vertra Hand Sanitizer topical solution by is a Otc medication manufactured, distributed, or labeled by Guangdong Longtai Industry Co.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 80%v/v

Purpose

Antiseptic

Uses

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

Warnings

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

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

Directions

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

Other information

Store between 15-20C(59-86F)
Coid freezing and excessive hear about 40C(104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

VERTRA HAND SANITIZER TOPICAL SOLUTION 
hand sanitizer topical solution liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52807-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52807-103-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
2	NDC: 52807-103-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
3	NDC: 52807-103-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
4	NDC: 52807-103-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
5	NDC: 52807-103-05	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
6	NDC: 52807-103-06	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
7	NDC: 52807-103-07	360 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
8	NDC: 52807-103-08	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
9	NDC: 52807-103-09	960 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020
10	NDC: 52807-103-10	1920 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/06/2020

Labeler - Guangdong Longtai Industry Co.,LTD (528076517)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Longtai Industry Co.,LTD		528076517	manufacture(52807-103)