HAND SANITIZER PLUS ALOE VERA- ethyl alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Jocott Brands, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 65%

PURPOSE

ANTIMICROBIAL

USE

• HAND SANITIZER CAN HELP REDUCE BACTERIA ON THE SURFACE OF SKIN.

WARNINGS

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION OR RASH APPEARS AND LASTS.

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

• APPLY PRODUCT ALL OVER HANDS UNTIL DRY.
• CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.

OTHER INFORMATION

• STORE BELOW 110°F (43°C)
• MAY DISCOLOR CERTAIN FABRICS OR SURFACES

INACTIVE INGREDIENTS

Purified Water (Aqua), PEG-6, Glycerin, Tocopheryl Acetate (Vitamin E), Aloe Barbadensis (Aloe Vera) Leaf Juice, Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER  PLUS ALOE VERA
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78902-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78902-105-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
2	NDC: 78902-105-32	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
3	NDC: 78902-105-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
4	NDC: 78902-105-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
5	NDC: 78902-105-06	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
6	NDC: 78902-105-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020
7	NDC: 78902-105-24	739 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/25/2020

Labeler - Jocott Brands, Inc. (080399826)