HAND SANITIZER- ethyl alcohol gel 
NingBo Laiao Daily Chemical 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.

----------

76897-001 ​Hand Sanitizer 62% Alcohol

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

Decreases bacteria on hands

For external use only

Do not use ■on broken skin & around eyes

When using this product

■Keep away from fire or flame

■Using other topical acne drugs at the same time or right

after use of this product may increase dryness or irritation of

the skin . Only one drug should be used unless directed by a

doctor.

Stop use and ask a doctor if rash occurs

Keep out of reach of children .If swallowed ,get medical

help or contact a Poison on Control Center immediately

Directions

Squeeze onto hands and rub hands and rub hands

together briskly until dry

Inactive ingredients

Deionized Water, Carbomer， Triethanolamine,Aloe

barbadensis Gel,Fragrance ，Glycerin, Propylene Glycol,

Vitamin E

1

HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76897-001
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76897-001-0110 in 1 CARTON05/20/2020
150 in 1 BOX
110 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:76897-001-0210 in 1 CARTON05/20/2020
250 in 1 BOX
212 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:76897-001-034 in 1 CARTON05/20/2020
350 in 1 BOX
315 mL in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:76897-001-042 in 1 CARTON05/20/2020
4125 in 1 BOX
420 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:76897-001-052 in 1 CARTON05/20/2020
5100 in 1 BOX
530 mL in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:76897-001-062 in 1 CARTON05/20/2020
6100 in 1 BOX
650 mL in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:76897-001-072 in 1 CARTON05/20/2020
7100 in 1 BOX
760 mL in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:76897-001-082 in 1 CARTON05/20/2020
850 in 1 BOX
8100 mL in 1 BOTTLE; Type 0: Not a Combination Product
9NDC:76897-001-092 in 1 CARTON05/20/2020
925 in 1 BOX
9236 mL in 1 BOTTLE; Type 0: Not a Combination Product
10NDC:76897-001-1024 in 1 CARTON05/20/2020
10500 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/20/2020
Labeler - NingBo Laiao Daily Chemical Co, Ltd. (554532225)
Establishment
NameAddressID/FEIBusiness Operations
NingBo Laiao Daily Chemical Co, Ltd.554532225manufacture(76897-001)

Revised: 5/2020
Document Id: a67721e5-4896-4f9c-e053-2a95a90ad2b2
Set id: a6772258-df78-803c-e053-2995a90a9b06
Version: 1
Effective Time: 20200525
 
NingBo Laiao Daily Chemical Co, Ltd.