KERICURE HAND SANITIZER- alcohol spray

KeriCure Hand Sanitizer by

Drug Labeling and Warnings

KeriCure Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Kericure Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Alcohol 70% (v/v)

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Warnings

For external use only Flammable, keep away from heat or flame Do not use on children less than 2 month of age  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

Keep out of reach of children Do NOT ingest If swallowed, seek medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions Shake bottle before use Spray enough product on hands to cover all surfaces Rub hands together until dry Adult supervision

STORAGE AND HANDLING

Other Information  Do not store bottle above 105°F May discolor some fabrics harmful to some wood finishes

INACTIVE INGREDIENT

Inactive Ingredients Water, isopropyl alcohol, aloe barbadensis, glycerin, natural fragrances, tocophoryl acetate, cellulose

SPL UNCLASSIFIED SECTION

■ LAVENDER ■ PEPPERMINT

MEDICAL

Made in the USA

KILLS MORE THAN 99.9% OF GERMS

FORMULATED FOR PROFESSIONALS

GENTLE ENOUGH FOR EVERYDAY USE

WITH ALOE & VITAMIN E

SKIN MOISTURIZERS

KeriCureMedical.com

® KeriCure Inc All rights reserved

Distributed by KeriCure Inc 3701A Southwestern Blvd. Baltimore MD 21229

Packaging

INGREDIENTS AND APPEARANCE

KERICURE HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78280-304
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78280-304-02	55 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/10/2020
2	NDC: 78280-304-08	230 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/10/2020	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/10/2020

Labeler - Kericure Inc. (966638681)