ZIVA HAND SANITIZER- alcohol spray

ZIVA HAND SANITIZER by

Drug Labeling and Warnings

ZIVA HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Ziva Wetwipes FZCo, Dirra USA, Ziva Wetwipes FZCO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (s)

Ethyl Alcohol 80% V/V

Purpose

Antiseptic

Use(s)

Hand sanitizer gives protection from bacteria & germs.

Use when soap and water are not available

Warnings

-For external use only.
-Flammable, keep away from the flames.

DO NOT USE

If irritation and skin redness develop.
On open skin wounds

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

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

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.

KEEP OUT OF REACH OF CHILDREN

Storage

Store between 15-30° C (59-86° F)
Avoid freezing and excessive heat above 40° C (104° F)

Inactive Ingredients.

Aqua, Glycerin, Tocopheryl Acetate (Vitamin E).

Product label

INGREDIENTS AND APPEARANCE

ZIVA HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81450-004
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
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81450-004-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/24/2021

Labeler - Ziva Wetwipes FZCo (559186188)

Registrant - Dirra USA (117678868)

Establishment
Name	Address	ID/FEI	Business Operations
Ziva Wetwipes FZCO		559186188	manufacture(81450-004)