My Little Pony(MLP 102)Hand Sanitizer

Manufacturer: Gold Orient International Limited
Effective date: 2020-07-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:03

Label at a glance#

ProductMy Little Pony(MLP 102)Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Store between 66 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(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% v/v.

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

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

Do not get into eyes.

if contact occurs, rinse eyes thoroughly with water

OTC - STOP USE SECTION

irritation and redness develop

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

wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Store between 66 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 Acrylates Crosspolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, Red 40

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL ARTWORK

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
51522-028-01	2022-01-28	C162847	48780-1	d6a99b39-4352-a426-e053-dadaa90af4c2	aae2f675-218a-c178-e053-2a95a90ad013

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51522-028-01	My Little Pony(MLP 102)Hand Sanitizer	30 mL in 1 BOTTLE, PLASTIC	GEL	30		1
51522-028-01	My Little Pony(MLP 102)Hand Sanitizer	1 in 1 POUCH	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51522-028	MY LITTLE PONY(MLP 102)HAND SANITIZER (ALCOHOL) GEL [GOLD ORIENT INTERNATIONAL LIMITED]	1	Legacy NDC, 2 package rows	20200721_aae2f675-218a-c178-e053-2a95a90ad013.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

My Little Pony(MLP 102)Hand Sanitizer
ALCOHOL
FD&C RED NO. 40
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
GLYCERIN
WATER
POLYSORBATE 20
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51522-028	51522-028-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
FD&C RED NO. 40	WZB9127XOA	IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
POLYSORBATE 20	7T1F30V5YH	IACT
SODIUM HYDROXIDE	55X04QC32I	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
aae2f675-217a-c178-e053-2a95a90ad013			aae2f675-218a-c178-e053-2a95a90ad013	2020-07-20	Warnings	Exact identifier spl id: aae2f675-217a-c178-e053-2a95a90ad013 spl set id: aae2f675-218a-c178-e053-2a95a90ad013

Reported adverse events (FAERS/openFDA)#

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