knDR SANITIZER

Manufacturer: CROP BEAUTY GROUP INC. | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:57:45

Label at a glance#

ProductknDR SANITIZER

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic.

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flame

When using this product

OTC - WHEN USING SECTION

Avoid the eyes and mucous membranes.
In the case of eyes or mucous membranes contact,rinse area thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens.
Redness or irritation develops.
Condition persists for more than 3 days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed,contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

Store below 105 °F.
May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Extract, Carbomer, Aminomethyl Propanol, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	2
581660	ethanol 0.62 ML/ML Topical Gel	SCD	2
581660	ethanol 62 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78768-004-30	knDR SANITIZER	30 mL in 1 TUBE	GEL	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78768-004	KNDR SANITIZER (ALCOHOL) GEL [CROP BEAUTY GROUP INC.]	2	Current NDC, Legacy NDC, 1 package rows	20231026_97f125d7-9ee9-4a0e-99e8-798df7ebb0ff.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

knDR SANITIZER
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78768-004	78768-004-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
ALCOHOL	3K9958V90M	ACTIB

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
knDR SANITIZER	ALCOHOL	CROP BEAUTY GROUP INC.	97f125d7-9ee9-4a0e-99e8-798df7ebb0ff	2023-10-26	Warnings	Exact identifier ndc (package): 78768-004-30 ndc (product): 78768-004 ndc11 (package): 78768000430 spl id: 0897b5ff-cabe-5ed5-e063-6294a90a92ee spl set id: 97f125d7-9ee9-4a0e-99e8-798df7ebb0ff

Reported adverse events (FAERS/openFDA)#

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