My Little Pony Hand Sanitizer

Manufacturer: Gold Orient International Limited
Effective date: 2020-07-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:33

Label at a glance#

ProductMy Little Pony Hand Sanitizer

Active ingredientALCOHOL

Label structure8 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 Denat. 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

When using this product

WARNINGS SECTION

do not get into eyes.
if contact occurs, rinse eyes thorouly with water

Stop use and ask a doctor if

WARNINGS SECTION

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

SPL UNCLASSIFIED SECTION

Store at 68° to 77°F (20°~25°C)
Do not store above 110°F (43°C)
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, Yellow 5, Blue 1.

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
51522-040-01	2022-01-28	C162847	48780-1	d6a99b39-5d43-a426-e053-dadaa90af4c2	My Little Pony(MLP 100) Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51522-040-01	My Little Pony Hand Sanitizer	1 in 1 POUCH	GEL	1		1
51522-040-01	My Little Pony Hand Sanitizer	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
51522-040	MY LITTLE PONY HAND SANITIZER (ALCOHOL DENAT.) GEL [GOLD ORIENT INTERNATIONAL LIMITED]	1	Legacy NDC, 2 package rows	20200725_ab142fce-baec-5db2-e053-2995a90a06b4.zip

Products#

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

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

My Little Pony Hand Sanitizer
Alcohol Denat.
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
WATER
ALCOHOL
POLYSORBATE 20
SODIUM HYDROXIDE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51522-040	51522-040-01

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 COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
POLYSORBATE 20	7T1F30V5YH	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
GLYCERIN	PDC6A3C0OX	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
ab142fce-baed-5db2-e053-2995a90a06b4			ab142fce-baec-5db2-e053-2995a90a06b4	2020-07-24	Warnings	Exact identifier spl id: ab142fce-baed-5db2-e053-2995a90a06b4 spl set id: ab142fce-baec-5db2-e053-2995a90a06b4

Reported adverse events (FAERS/openFDA)#

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