ASSORTED LICENSED HAND SANITIZER GRAPE 01- alcohol spray 
Shenzhen Lantern Scicence Co.,Ltd.

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Assorted Licensed Hand Sanitizer

Drug Facts

drug factsDrug Facts

Active Ingredient

Active ingredient Purpose

Ethyl Alcohol 70% v/v Antiseptic

Uses

Decreases bacieria on skin

Warning

For external use only

Do not use

lf you are allergic to any of the ingredients

When using this product

Do not get into eyes. lf contact occurs, rinse thoroughly with water.Do not use in or near eyes,In case of eye contact ,flush eyes thoroughly with water. Discontinue if skin becomes irritated and ask for a doctor.

Stop use and ask a doctor

lf irritation or rash develops and continues for more than72 hours.

keep out of reach of children

lf swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 6 years and older
Spray onto hands and rub together unil dry. Recommended for repeat use.
Children under 6 years of age
should be supervised when using this product.

Inactive ingredients

Water, Fragrance,Glycerin, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Gel, Denatonium Benzoate.

other Information


Storebetween15-30C(59-86F)
Avoid freezing and excessive heat above 40C (104F)

Spray 3-4 times each time.
Used in the skin area of the hands.

packing

packingpacking

ASSORTED LICENSED HAND SANITIZER GRAPE  01
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-423
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54860-423-0128 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00307/06/2024
Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)
Establishment
NameAddressID/FEIBusiness Operations
Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-423)

Revised: 7/2024
Document Id: 1c90a1ac-485e-fdd1-e063-6394a90a5cdf
Set id: 1c9095ad-ce19-3666-e063-6394a90ae22d
Version: 1
Effective Time: 20240709
 
Shenzhen Lantern Scicence Co.,Ltd.