NIFOLA HAND SANITIZER WITH ALOE VERA AND VITAMIN E- alcohol gel 
Yiwu Yangjie Daily Chemicals 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                70%  V/V    ...   Antiseptic

if swallowed, get meical help or contact a poison control center right away.

Dispense a small amount on palms. Rub lightly until dry. Do not rinse.

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

Avoid contact with eyes, in case of contact, rinse with water immediately.

If irritation develops, discontinue use and consult a doctor.

OTHER INFORMATION: store under 105℉.

Dispense a small amount on palms. Rub lightly until dry. Do not rinse.

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

image of label

NIFOLA HAND SANITIZER WITH ALOE VERA AND VITAMIN E 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74149-022
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
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74149-022-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
2NDC:74149-022-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
3NDC:74149-022-0353 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
4NDC:74149-022-04236 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
5NDC:74149-022-05500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/12/2020
Labeler - Yiwu Yangjie Daily Chemicals Co.,Ltd. (529648827)
Establishment
NameAddressID/FEIBusiness Operations
Yiwu Yangjie Daily Chemicals Co.,Ltd.529648827manufacture(74149-022)

Revised: 6/2020
Document Id: 4bfa79e1-3e85-445b-947d-9ae92d7eb86a
Set id: 1d43eed8-11d8-48b3-9900-ef9a4e65f70e
Version: 1
Effective Time: 20200612
 
Yiwu Yangjie Daily Chemicals Co.,Ltd.