PEARLESSENCE SANITIZING WIPES

Manufacturer: Jocott Brands, Inc.
Effective date: 2020-11-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:33:19

Label at a glance#

ProductPEARLESSENCE SANITIZING WIPES

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

APPLY PRODUCT ALL OVER HANDS UNTIL DRY. CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.

Storage and handling

STORE BELOW 110°F (43°C) MAY DISCOLOR CERTAIN FABRICS OR SURFACES

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 75%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USE

INDICATIONS & USAGE SECTION

HAND SANITIZER CAN HELP REDUCE BACTERIA ON THE SURFACE OF SKIN.

WARNINGS

WARNINGS SECTION

FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION OR RASH APPEARS AND LASTS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY PRODUCT ALL OVER HANDS UNTIL DRY.
CHILDREN SHOULD BE SUPERVISED AT ALL TIMES WHEN USING THIS PRODUCT.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE BELOW 110°F (43°C)
MAY DISCOLOR CERTAIN FABRICS OR SURFACES

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified Water (Aqua), Aloe Barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate (Vitamin E)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Pearlessence_Hand Sani Wipes_160ct

01b LBL_Pearlessence_Hand Sani Wipes_50ct

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78902-302-51	2021-07-23	C162847	48780-1	c7ccaba7-2adb-fd44-e053-dadaa90aa01b	PEARLESSENCE - SANITIZING WIPES - 75% Ethyl Alcohol
78902-302-52	2021-07-23	C162847	48780-1	c7ccaba7-2adb-fd44-e053-dadaa90aa01b	PEARLESSENCE - SANITIZING WIPES - 75% Ethyl Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
78902-302-11	PEARLESSENCE SANITIZING WIPES	1 in 1 APPLICATOR	SOLUTION	1	1
78902-302-51	PEARLESSENCE SANITIZING WIPES	160 in 1 CONTAINER	SOLUTION	160	1
78902-302-52	PEARLESSENCE SANITIZING WIPES	50 in 1 CONTAINER	SOLUTION	50	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78902-302	PEARLESSENCE SANITIZING WIPES (ETHYL ALCOHOL) SOLUTION [JOCOTT BRANDS, INC.]	1	Legacy NDC, 3 package rows	20201110_e477e281-8476-4cfd-9c58-2881884ca0b8.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

PEARLESSENCE SANITIZING WIPES
ETHYL ALCOHOL
ALCOHOL
WATER
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78902-302	78902-302-11, 78902-302-51, 78902-302-52

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
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	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
c268e389-7ff6-4fd5-9867-d0bc9fda81c5			e477e281-8476-4cfd-9c58-2881884ca0b8	2020-11-09	Warnings	Exact identifier spl id: c268e389-7ff6-4fd5-9867-d0bc9fda81c5 spl set id: e477e281-8476-4cfd-9c58-2881884ca0b8

Reported adverse events (FAERS/openFDA)#

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