MELLOW HAND SANITIZER (ALOE AND VITAMIN E)- alcohol gel 
Ningbo Liyuan Daily Chemical Products 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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Drug facts

Active ingredient                                  Purpose

Ethyl Alcohol                62%      ...        Antiseptic

Hand sanitizer to help decrease bacteria on the skin.

If swallowed, get medical help or contact local poison control center right away.

Children must be supervised in use of this product.

keep out of eyes

when water, soap and towel are not available

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

Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

Stop using and ask a doctor, if irritation and redness develops, if condition persists for more than 72 hours, consult a doctor.

Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry.

Water, Carbomer, Glycerin, Propylene Glycol, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance

image of label

MELLOW HAND SANITIZER (ALOE AND VITAMIN E) 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) alcohol62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER 934 (UNII: Z135WT9208)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76176-301-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2017
2NDC:76176-301-02236 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/16/2017
Labeler - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)
Registrant - Ningbo Liyuan Daily Chemical Products Co.,Ltd. (530766098)
Establishment
NameAddressID/FEIBusiness Operations
Ningbo Liyuan Daily Chemical Products Co.,Ltd.530766098manufacture(76176-301)

Revised: 6/2017
Document Id: 83c850c5-8f3e-482c-895e-a5d52f95d5f2
Set id: 6ebac2ad-f829-41eb-a272-68ed8c4fe5a4
Version: 1
Effective Time: 20170616
 
Ningbo Liyuan Daily Chemical Products Co.,Ltd.