FDA.reportPublic FDA data

Blue Cedar Hand Sanitizer

Manufacturer
Anhui Kiwi Biotech Co., Ltd.
Effective date
2020-04-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:06

Label at a glance#

ProductBlue Cedar Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store below 110°F (43° C).
May discolor certain fabrics or surfaces.

WARNINGS SECTION

Flammable. Keep away from fire or flame.

Forexternal use only.

Do not use this product in or near the eyes. In case of accidental contact, ninse eyes thoroughly with water.

Stop use and ask doctor if iritation or rash appears andlasts.

Keep away from children. If sallowed, get medicalhelp right away,

OTC - PURPOSE SECTION

Kills Harmful Bacteria or Germs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children.

INDICATIONS & USAGE SECTION

Place enough product (1.5~-2 mL, about one full pump) in your palm to thoroughly cover your hands.

Rub hands briskly until dry.

Children under 6 years old should be supervised when using this product.

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75土 59% 6(VW) or 65士5%

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycereth :26, Triethanolamine, Fragrance (Parfum).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55444-003-012021-07-23C16284748780-1c7ccaba7-1e33-fd44-e053-dadaa90aa01ba405bdf1-019a-0821-e053-2995a90a49a2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55444-003-01Blue Cedar Hand Sanitizer200 mL in 1 BOTTLEGEL2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55444-003BLUE CEDAR HAND SANITIZER (HAND SANITIZER) GEL [ANHUI KIWI BIOTECH CO., LTD.]2Legacy NDC, 1 package rows20200427_a405bdf1-019a-0821-e053-2995a90a49a2.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55444-00355444-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
.ALPHA.-TERPINEOL21334LVV8WIACT
TERPINEOLR53Q4ZWC99IACT
.GAMMA.-NONALACTONEI1XGH66S8PIACT
LINALOOL, (+/-)-D81QY6I88EIACT
METHYL DIHYDROJASMONATE (SYNTHETIC)3GW44CIE3YIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
GLYCERETH-26NNE56F2N14IACT
PHENYLETHYL ALCOHOLML9LGA7468IACT

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
a4349d07-8688-6e31-e053-2a95a90a6f54a405bdf1-019a-0821-e053-2995a90a49a22020-04-26WarningsExact identifier
spl id: a4349d07-8688-6e31-e053-2a95a90a6f54
spl set id: a405bdf1-019a-0821-e053-2995a90a49a2