NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE- alcohol solution

NexSense Liquid Hand Sanitizer Moisturizing with Aloe by

Drug Labeling and Warnings

NexSense Liquid Hand Sanitizer Moisturizing with Aloe by is a Otc medication manufactured, distributed, or labeled by Taizhou Yadai Daily-Use Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 62% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria on the skin

Recommended for repeated use

Warnings

For external use only. Flammable. Keep away from fire or flame

Do not apply around eyes or use in ears or mouth

Stop use and contact a doctor if redness or irritation develop or persist for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Directions

• Pump as needed into your palms and thoroughly spead on both hands
• rub into skin until dry

Other information

• Store at room temperature no higher than 45C (115F) and under shade
• Keep in closed containers and free from direct sunlight 

Inactive ingredients

Water, Glycerol, Aminomethyl propanol, Aloe Vera gel, Vitamin E, Carbomer, Frangrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52989-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER 934 (UNII: Z135WT9208)
TROLAMINE (UNII: 9O3K93S3TK)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52989-003-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/19/2020
2	NDC: 52989-003-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/19/2020
3	NDC: 52989-003-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/19/2020

Labeler - Taizhou Yadai Daily-Use Co., Ltd. (529899639)

Establishment
Name	Address	ID/FEI	Business Operations
Taizhou Yadai Daily-Use Co., Ltd.		529899639	manufacture(52989-003)