ZAPIRE HAND SANITIZER- ethyl alcohol gel

ZAPIRE HAND SANITIZER by

Drug Labeling and Warnings

ZAPIRE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Natural Dyes Inc, PUJIANG SHIJIALI COSMETICS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin that could cause disease.
• When water, soap and towel are not available.
• Recommended for repeated use.

Warnings

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product  Keep out of eyes, ears, or mouth.  In case of eye contact, flush eyes thoroughly with water.  Avoid contact with broken skin.  Do not inhale or ingest.

Stop use and ask a doctor if  redness or irritation develop

condition persists for more than 72 hours

Keep out of reach of children.

Children should be supervised by an adult when using this product.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hand thoroughly with product and allow to dry without wiping.  No rinsing required.  For children under 6, use only under adult supervision.  Not recommended for infants.

Other information

Store below 105˚F(40˚C).  May discolor certain fabrics.  Harmful to wood finishes & plastics

Inactive ingredients:

Water(Aqua), Triethanolamine, Carbomer, Aloe Barbadensis(Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate(Vitamin E).

SPL UNCLASSIFIED SECTION

UPC CODE

Distributed by:

Natural Dyes Inc.

New York, NY 10018

Made in China

Kills 99.9% of Germs

Moisturizing Formula

70% Alcohol 

Sanitary

Aloe

E

Vitamin E

Packaging

INGREDIENTS AND APPEARANCE

ZAPIRE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77781-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77781-002-02	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/30/2020

Labeler - Natural Dyes Inc (078772235)

Establishment
Name	Address	ID/FEI	Business Operations
PUJIANG SHIJIALI COSMETICS CO., LTD.		529748603	manufacture(77781-002)