CHOBS-READY TO HAND SANITIZER

Manufacturer
CH Harmony Co., Ltd.
Effective date
2020-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:47

Label at a glance#

ProductCHOBS-READY TO HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

water, glycerin, triethanolamine, etc

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.

Supervise children in the use of this product.

WARNINGS SECTION

For external use only.

Flammable.

Keep away from fire or flame.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74122-0010-12021-07-23C16284748780-1c7ccaba7-1a61-fd44-e053-dadaa90aa01bCH Harmony Co., Ltd. - CHOBS-READY TO HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74122-0010-1CHOBS-READY TO HAND SANITIZER100 mL in 1 TUBEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74122-0010CHOBS-READY TO HAND SANITIZER (ALCOHOL) GEL [CH HARMONY CO., LTD.]1Legacy NDC, 1 package rows20200402_a24b40cc-fe1f-c456-e053-2a95a90aa0fc.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74122-001074122-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a24b5226-11c2-fc52-e053-2995a90a55d6a24b40cc-fe1f-c456-e053-2a95a90aa0fc2020-04-02WarningsExact identifier
spl id: a24b5226-11c2-fc52-e053-2995a90a55d6
spl set id: a24b40cc-fe1f-c456-e053-2a95a90aa0fc

Reported adverse events (FAERS/openFDA)#

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