FOAMING MOUSSE ANTI-BACTERIAL HAND SANITIZER CHERRY SCENTED- alcohol aerosol, foam 
Ganzhou Olivee Cosmetic 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

Alcohol                62%      ...                Antiseptic

Decrease bacteria on hands.

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

Avoid contact with eyes， if contact occurs rinse thoroughly with water.

For external use only.
Flammable. Keep product away from flame or high heat. contents under pressure. Do not puncture or in cinerate.

Stop using and ask a doctor, if irritation and redness develop or increase.

shake well before using; dispense a golf bass size amount in to hands; rub until dry.

Water (aqua), Carbomer, Sodium laureth sulfate, Glycerin, Coco-glucoside, Isopropyl palmitate, Sodium laureyl sarcosinate, Hydroxypropyl guar, Hydroxypropyl trimonium chloride, Prunus amygdalus dulcis (sweet almond) oil, Fragrance (parfum).

image of label

FOAMING MOUSSE ANTI-BACTERIAL HAND SANITIZER  CHERRY SCENTED
alcohol aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56136-021
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)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
CARBOMER 934 (UNII: Z135WT9208)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCO GLUCOSIDE (UNII: ICS790225B)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
HYDROXYPROPYL GUAR (2500-4500 MPA.S AT 1%) (UNII: 3A1I7376TC)  
HYDROXYPROPYL TRIMONIUM CHLORIDE (UNII: 8XE51CV5DE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:56136-021-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product11/28/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/28/2018
Labeler - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)
Registrant - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)
Establishment
NameAddressID/FEIBusiness Operations
Ganzhou Olivee Cosmetic Co., Ltd.543008195manufacture(56136-021)

Revised: 11/2018
Document Id: 7ed0bf57-ddd2-4864-a95f-f0dd7fa0b511
Set id: 35bd0f8f-1602-4713-b20f-8dc38e2761c2
Version: 1
Effective Time: 20181128
 
Ganzhou Olivee Cosmetic Co., Ltd.