CHOICE HAND SANITIZE- ethyl alcohol gel

Choice by

Drug Labeling and Warnings

Choice by is a Otc medication manufactured, distributed, or labeled by Inopak. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

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. Children should be supervised by an adult when using this product.

Usage

Uses

• To decrease bacteria on the skin that potentially can cause disease
• Recommended for repeated use

Warnings

Warnings

• Flammable, keep away from heat or flame.
• For external use only.

Other Information

Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water

May discolor certain fabrics and surfaces.

Stop Usage

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Administration

Directions

• Apply sufficient amount of product to your palm to cover both hands.
• Rub until dry.

Inactive Ingredients

Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

Choice Box Container

Drug Facts Active Ingredient                             Purpose Ethyl Alcohol 70% v/v ……………Antiseptic Uses To decrease bacteria on the skin that potentially can cause disease Recommended for repeated use Warnings Flammable, keep away from heat or flame. For external use only. Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed. Get medical help or contact a Poison Control Center right away. Children should be supervised by an adult when using this product. Directions Apply sufficient amount of product to your palm to cover both hands. Rub until dry. Other Information May discolor certain fabrics and surfaces. Inactive Ingredients Acrylates/C 10/30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue 1, FD&C Yellow 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water	Choice HAND SANITIZING GEL Aloe Ver   And Vitamin E Instant Waterless Contains Moisturizers PN 5025-404UV-CH 800m	Hand sanitizing gel Contains Aloe Vera and Vitamin E Instant waterless with moisturizers Produced in an FDA registered facility cGMP facility Dries quickly leaving the skin feeling soothed and moisturized Kills 99.9% of Germs MADE IN THE USA	Choice Dispenser Loading Instructions

      Section 1                                 Section 2                           Section 3                           Section 4

Choice Case

                                                                                5025-CH-CS         Rev. 1.0

Choice™

HAND SANITIZING GEL                   Kills 99.9% of Germs

Instant Waterless                             Aloe Ver and Vitamin E

Contains Moisturizers

MADE IN THE USA                           5025-404UV-CH

                                                                12/800 ML UV                   040232 65077 2

INGREDIENTS AND APPEARANCE

CHOICE  HAND SANITIZE
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58575-183
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
ALOE (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58575-183-01	800 mL in 1 POUCH; Type 0: Not a Combination Product	01/02/2020
2	NDC: 58575-183-02	9600 mL in 1 CASE; Type 0: Not a Combination Product	01/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/02/2020

Labeler - Inopak. Ltd (194718243)

Establishment
Name	Address	ID/FEI	Business Operations
Inopak. Ltd		194718243	manufacture(58575-183)