NEXSENSE LIQUID HAND SANITIZER MOISTURIZING WITH ALOE- alcohol solution
Taizhou Yadai Daily-Use Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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52989-003

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. 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

image description

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

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

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

#	Item Code	Package Description	Marketing Start Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/19/2020

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

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