Wish Ultra hand sanitizer dream in cherry blossoms by Zhejiang Meizhiyuan Cosmetics Co.,Ltd

Wish Ultra hand sanitizer dream in cherry blossoms by

Drug Labeling and Warnings

Wish Ultra hand sanitizer dream in cherry blossoms by is a Otc medication manufactured, distributed, or labeled by Zhejiang Meizhiyuan Cosmetics Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WISH ULTRA HAND SANITIZER DREAM IN CHERRY BLOSSOMS- alcohol gel 
Zhejiang Meizhiyuan Cosmetics 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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Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria on the skin that may cause disease.

Warnings

For external use only. Flammable. Keep away from heat and flame.
When using this product avoid contat with face, eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. children should be supervised by an adult when using this product.

Apply as needed. Store at room temperature below 110 oF (43 oC)

Inactive ingredients

Water (Aqua), Propylene Glycol, Glycerin,Carbomer, Fragrance, Aminomethyl Propanol, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E, Lactose, Zea Mays corn starch, Sucrose, Microcrystalline cellose, Hydroxylpropyl Methylcellulose, Ultramarines(I77007), FD&C Red No.40.

Package Label - Principal Display Panel

WISH ULTRA HAND SANITIZER DREAM IN CHERRY BLOSSOMS 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80204-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
STARCH, CORN (UNII: O8232NY3SJ)
SUCROSE (UNII: C151H8M554)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
HYPROMELLOSE 2208 (100000 MPA.S) (UNII: VM7F0B23ZI)
ULTRAMARINE BLUE (UNII: I39WR998BI)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80204-030-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/28/2020	03/24/2024

Labeler - Zhejiang Meizhiyuan Cosmetics Co.,Ltd (543036597)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Meizhiyuan Cosmetics Co.,Ltd		543036597	manufacture(80204-030)

Revised: 11/2022

Document Id: a9fc8480-b8b6-4e6f-9714-a360a67734d9

34390-5

Set id: 142a69eb-2795-4a23-8ed4-2bd560e2c50e

Version: 3

Effective Time: 20221118