Codi HAND SANITIZER

Manufacturer: YOUSU trading | Soriso
Effective date: 2020-05-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:14:48

Label at a glance#

ProductCodi HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water

Glycerin

Butylene Glycol

Carbomer

Triethanolamine

Mulberry Root Extract

Ginseng Extract

Aloe Extract

Allantoin

Tocopheryl Acetate

Tea Tree Oil

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

For the external use only

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

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

DOSAGE & ADMINISTRATION SECTION

Place enough product on hand to cover all surfaces. Rub hands together until dry. Children under 6 years should be supervised when using this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78296-0001-1	2021-07-23	C162847	48780-1	c7ccaba7-1488-fd44-e053-dadaa90aa01b	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78296-0001-1	Codi HAND SANITIZER	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78296-0001	CODI HAND SANITIZER (ALCOHOL) GEL [YOUSU TRADING]	1	Legacy NDC, 1 package rows	20200527_a6877612-df62-0cbe-e053-2995a90a729e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Codi HAND SANITIZER
Alcohol
GLYCERIN
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
BUTYLENE GLYCOL
ALOE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78296-0001	78296-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALOE	V5VD430YW9	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a687761b-eb53-00a3-e053-2a95a90a619e			a6877612-df62-0cbe-e053-2995a90a729e	2020-05-26	Warnings	Exact identifier spl id: a687761b-eb53-00a3-e053-2a95a90a619e spl set id: a6877612-df62-0cbe-e053-2995a90a729e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.