ACORE Peppermint Hand Sanitizer

Manufacturer: Gold Orient International Limited
Effective date: 2020-07-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:45

Label at a glance#

ProductACORE Peppermint Hand Sanitizer Boys

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store at 68 to 77F (20-25C) Do not store above 110F (43C) You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use for hand-washing to decrease bacteria on the skin, only when water it not available.

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire and flames.

When using this product

OTC - WHEN USING SECTION

Do not get into eyes.

If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

If irritation and redness develop.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Store at 68 to 77F (20-25C)

Do not store above 110F (43C)

You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,

Glycerin,

Acrylates/C10-30 Alkyl Acrylate Crosspolymer,

Fragrance,

Polysorbate 20,

Sodium Hydroxide,

Blue 1,

Yellow 5

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51522-044-01	2022-01-28	C162847	48780-1	d6a99b39-92ed-a426-e053-dadaa90af4c2	ACORE Peppermint（Boys）Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51522-044-01	ACORE Peppermint Hand SanitizerBoys	1 in 1 CASE	GEL	1		1
51522-044-01	ACORE Peppermint Hand SanitizerBoys	30 mL in 1 BOTTLE, PLASTIC	GEL	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51522-044	ACORE PEPPERMINT HAND SANITIZER BOYS (ALCOHOL DENAT.) GEL [GOLD ORIENT INTERNATIONAL LIMITED]	1	Legacy NDC, 2 package rows	20200815_abb3c3ff-c1cf-e36a-e053-2a95a90a5738.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

ACORE Peppermint Hand Sanitizer Boys
Alcohol Denat.
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
FD&C BLUE NO. 1
POLYSORBATE 20
FD&C YELLOW NO. 5
GLYCERIN
ALCOHOL
SODIUM HYDROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51522-044	51522-044-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
SODIUM HYDROXIDE	55X04QC32I	IACT
WATER	059QF0KO0R	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
abb3c3ff-c1d0-e36a-e053-2a95a90a5738			abb3c3ff-c1cf-e36a-e053-2a95a90a5738	2020-07-31	Warnings	Exact identifier spl id: abb3c3ff-c1d0-e36a-e053-2a95a90a5738 spl set id: abb3c3ff-c1cf-e36a-e053-2a95a90a5738

Reported adverse events (FAERS/openFDA)#

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